Principles of asymmetric synthesis:
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
Oxford, U.K. ; Tarrytown, N.Y.
Pergamon
1996
|
| Ausgabe: | 1st ed |
| Schriftenreihe: | Tetrahedron organic chemistry series
v. 14 |
| Schlagworte: | |
| Beschreibung: | Print version record |
| Beschreibung: | 1 online resource (xvii, 372 pages) illustrations |
| ISBN: | 9780080514772 0080514774 9780080418759 0080418759 |
Internformat
MARC
| LEADER | 00000nmm a2200000zcb4500 | ||
|---|---|---|---|
| 001 | BV045342992 | ||
| 003 | DE-604 | ||
| 005 | 00000000000000.0 | ||
| 007 | cr|uuu---uuuuu | ||
| 008 | 181206s1996 |||| o||u| ||||||eng d | ||
| 020 | |a 9780080514772 |9 978-0-08-051477-2 | ||
| 020 | |a 0080514774 |9 0-08-051477-4 | ||
| 020 | |a 9780080418759 |9 978-0-08-041875-9 | ||
| 020 | |a 0080418759 |9 0-08-041875-9 | ||
| 035 | |a (ZDB-4-ENC)ocn316220611 | ||
| 035 | |a (OCoLC)316220611 | ||
| 035 | |a (DE-599)BVBBV045342992 | ||
| 040 | |a DE-604 |b ger |e rda | ||
| 041 | 0 | |a eng | |
| 082 | 0 | |a 547.2 |2 22 | |
| 100 | 1 | |a Gawley, Robert E. |e Verfasser |4 aut | |
| 245 | 1 | 0 | |a Principles of asymmetric synthesis |c Robert E. Gawley and Jeffrey Aube |
| 250 | |a 1st ed | ||
| 264 | 1 | |a Oxford, U.K. ; Tarrytown, N.Y. |b Pergamon |c 1996 | |
| 300 | |a 1 online resource (xvii, 372 pages) |b illustrations | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b c |2 rdamedia | ||
| 338 | |b cr |2 rdacarrier | ||
| 490 | 0 | |a Tetrahedron organic chemistry series |v v. 14 | |
| 500 | |a Print version record | ||
| 505 | 8 | |a The world is chiral. Most of the molecules in it are chiral, and asymmetric synthesis is an important means by which enantiopure chiral molecules may be obtained for study and sale. Using examples from the literature of asymmetric synthesis (more than 1300 references), the aim of this book is to present a detailed analysis of the factors that govern stereoselectivity in organic reactions. It is important to note that the references were each individually checked by the authors to verify relevance to the topics under discussion. The study of stereoselectivity has evolved from issues of diastereoselectivity, through auxiliary-based methods for the synthesis of enantiomerically pure compounds (diastereoselectivity followed by separation and auxiliary cleavage), to asymmetric catalysis. | |
| 505 | 8 | |a In the latter instance, enantiomers (not diastereomers) are the products, and highly selective reactions and modern purification techniques allow preparation - in a single step - of chiral substances in 99% ee for many reaction types. After an explanation of the basic physical-organic principles of stereoselectivity, the authors provide a detailed, annotated glossary of stereochemical terms. A chapter on "Analytical Methods" provides a critical overview of the most common methods for analysis of stereoisomers. The authors then follow the 'tried-and-true' format of grouping the material by reaction type. Thus, there are four chapters on carbon-carbon bond forming reactions (enolate alkylations, organometal additions to carbonyls, aldol and Michael reactions, and cycloadditions and rearrangements), one chapter on reductions and hydroborations (carbon-hydrogen bond forming reactions), and one on oxidations (carbon-oxygen and carbon-nitrogen bond forming reactions). | |
| 505 | 8 | |a Leading references are provided to natural product synthesis that have been accomplished using a given reaction as a key step. In addition to tables of examples that show high selectivity, a transition state analysis is presented to explain - to the current level of understanding - the stereoselectivity of each reaction. In one case (Cram's rule) the evolution of the current theory is detailed from its first tentative (1952) postulate to the current Felkin-Anh-Heathcock formalism. For other reactions, only the currently accepted rationale is presented. Examination of these rationales also exposes the weaknesses of current theories, in that they cannot always explain the experimental observations. These shortcomings provide a challenge for future mechanistic investigations. | |
| 505 | 8 | |a An http://www.sciencedirect.com/science/publication?issn=14601567 & volume=14<HREF>http://asnetserver.as.miami.edu/rgawley/Book.html</HREF><HTXT>updated list of references</HTXT></URL> for this book can also be viewed | |
| 650 | 7 | |a SCIENCE / Chemistry / Organic |2 bisacsh | |
| 650 | 7 | |a Asymmetric synthesis |2 fast | |
| 650 | 7 | |a Synthese (chemie) |2 gtt | |
| 650 | 7 | |a Chiraliteit |2 gtt | |
| 650 | 7 | |a Enantiomeren |2 gtt | |
| 650 | 7 | |a Synthese asymetrique |2 ram | |
| 650 | 7 | |a Composes organiques |2 ram | |
| 650 | 4 | |a Asymmetric synthesis | |
| 650 | 0 | 7 | |a Asymmetrische Synthese |0 (DE-588)4135603-2 |2 gnd |9 rswk-swf |
| 689 | 0 | 0 | |a Asymmetrische Synthese |0 (DE-588)4135603-2 |D s |
| 689 | 0 | |8 1\p |5 DE-604 | |
| 700 | 1 | |a Aube, Jeffrey |e Sonstige |4 oth | |
| 776 | 0 | 8 | |i Erscheint auch als |n Druck-Ausgabe |a Gawley, Robert E. |t Principles of asymmetric synthesis |b 1st ed |d Oxford, U.K. ; Tarrytown, N.Y. : Pergamon, 1996 |z 0080418767 |z 9780080418766 |
| 912 | |a ZDB-4-ENC | ||
| 999 | |a oai:aleph.bib-bvb.de:BVB01-030729695 | ||
| 883 | 1 | |8 1\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
Datensatz im Suchindex
| _version_ | 1804179161319735296 |
|---|---|
| any_adam_object | |
| author | Gawley, Robert E. |
| author_facet | Gawley, Robert E. |
| author_role | aut |
| author_sort | Gawley, Robert E. |
| author_variant | r e g re reg |
| building | Verbundindex |
| bvnumber | BV045342992 |
| collection | ZDB-4-ENC |
| contents | The world is chiral. Most of the molecules in it are chiral, and asymmetric synthesis is an important means by which enantiopure chiral molecules may be obtained for study and sale. Using examples from the literature of asymmetric synthesis (more than 1300 references), the aim of this book is to present a detailed analysis of the factors that govern stereoselectivity in organic reactions. It is important to note that the references were each individually checked by the authors to verify relevance to the topics under discussion. The study of stereoselectivity has evolved from issues of diastereoselectivity, through auxiliary-based methods for the synthesis of enantiomerically pure compounds (diastereoselectivity followed by separation and auxiliary cleavage), to asymmetric catalysis. In the latter instance, enantiomers (not diastereomers) are the products, and highly selective reactions and modern purification techniques allow preparation - in a single step - of chiral substances in 99% ee for many reaction types. After an explanation of the basic physical-organic principles of stereoselectivity, the authors provide a detailed, annotated glossary of stereochemical terms. A chapter on "Analytical Methods" provides a critical overview of the most common methods for analysis of stereoisomers. The authors then follow the 'tried-and-true' format of grouping the material by reaction type. Thus, there are four chapters on carbon-carbon bond forming reactions (enolate alkylations, organometal additions to carbonyls, aldol and Michael reactions, and cycloadditions and rearrangements), one chapter on reductions and hydroborations (carbon-hydrogen bond forming reactions), and one on oxidations (carbon-oxygen and carbon-nitrogen bond forming reactions). Leading references are provided to natural product synthesis that have been accomplished using a given reaction as a key step. In addition to tables of examples that show high selectivity, a transition state analysis is presented to explain - to the current level of understanding - the stereoselectivity of each reaction. In one case (Cram's rule) the evolution of the current theory is detailed from its first tentative (1952) postulate to the current Felkin-Anh-Heathcock formalism. For other reactions, only the currently accepted rationale is presented. Examination of these rationales also exposes the weaknesses of current theories, in that they cannot always explain the experimental observations. These shortcomings provide a challenge for future mechanistic investigations. An http://www.sciencedirect.com/science/publication?issn=14601567 & volume=14<HREF>http://asnetserver.as.miami.edu/rgawley/Book.html</HREF><HTXT>updated list of references</HTXT></URL> for this book can also be viewed |
| ctrlnum | (ZDB-4-ENC)ocn316220611 (OCoLC)316220611 (DE-599)BVBBV045342992 |
| dewey-full | 547.2 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547.2 |
| dewey-search | 547.2 |
| dewey-sort | 3547.2 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie |
| edition | 1st ed |
| format | Electronic eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>04753nmm a2200565zcb4500</leader><controlfield tag="001">BV045342992</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">181206s1996 |||| o||u| ||||||eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780080514772</subfield><subfield code="9">978-0-08-051477-2</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0080514774</subfield><subfield code="9">0-08-051477-4</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780080418759</subfield><subfield code="9">978-0-08-041875-9</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0080418759</subfield><subfield code="9">0-08-041875-9</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ZDB-4-ENC)ocn316220611</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)316220611</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV045342992</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rda</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">547.2</subfield><subfield code="2">22</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Gawley, Robert E.</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Principles of asymmetric synthesis</subfield><subfield code="c">Robert E. Gawley and Jeffrey Aube</subfield></datafield><datafield tag="250" ind1=" " ind2=" "><subfield code="a">1st ed</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Oxford, U.K. ; Tarrytown, N.Y.</subfield><subfield code="b">Pergamon</subfield><subfield code="c">1996</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (xvii, 372 pages)</subfield><subfield code="b">illustrations</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="490" ind1="0" ind2=" "><subfield code="a">Tetrahedron organic chemistry series</subfield><subfield code="v">v. 14</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Print version record</subfield></datafield><datafield tag="505" ind1="8" ind2=" "><subfield code="a">The world is chiral. Most of the molecules in it are chiral, and asymmetric synthesis is an important means by which enantiopure chiral molecules may be obtained for study and sale. Using examples from the literature of asymmetric synthesis (more than 1300 references), the aim of this book is to present a detailed analysis of the factors that govern stereoselectivity in organic reactions. It is important to note that the references were each individually checked by the authors to verify relevance to the topics under discussion. The study of stereoselectivity has evolved from issues of diastereoselectivity, through auxiliary-based methods for the synthesis of enantiomerically pure compounds (diastereoselectivity followed by separation and auxiliary cleavage), to asymmetric catalysis. </subfield></datafield><datafield tag="505" ind1="8" ind2=" "><subfield code="a">In the latter instance, enantiomers (not diastereomers) are the products, and highly selective reactions and modern purification techniques allow preparation - in a single step - of chiral substances in 99% ee for many reaction types. After an explanation of the basic physical-organic principles of stereoselectivity, the authors provide a detailed, annotated glossary of stereochemical terms. A chapter on "Analytical Methods" provides a critical overview of the most common methods for analysis of stereoisomers. The authors then follow the 'tried-and-true' format of grouping the material by reaction type. Thus, there are four chapters on carbon-carbon bond forming reactions (enolate alkylations, organometal additions to carbonyls, aldol and Michael reactions, and cycloadditions and rearrangements), one chapter on reductions and hydroborations (carbon-hydrogen bond forming reactions), and one on oxidations (carbon-oxygen and carbon-nitrogen bond forming reactions). </subfield></datafield><datafield tag="505" ind1="8" ind2=" "><subfield code="a">Leading references are provided to natural product synthesis that have been accomplished using a given reaction as a key step. In addition to tables of examples that show high selectivity, a transition state analysis is presented to explain - to the current level of understanding - the stereoselectivity of each reaction. In one case (Cram's rule) the evolution of the current theory is detailed from its first tentative (1952) postulate to the current Felkin-Anh-Heathcock formalism. For other reactions, only the currently accepted rationale is presented. Examination of these rationales also exposes the weaknesses of current theories, in that they cannot always explain the experimental observations. These shortcomings provide a challenge for future mechanistic investigations. </subfield></datafield><datafield tag="505" ind1="8" ind2=" "><subfield code="a">An http://www.sciencedirect.com/science/publication?issn=14601567 & volume=14<HREF>http://asnetserver.as.miami.edu/rgawley/Book.html</HREF><HTXT>updated list of references</HTXT></URL> for this book can also be viewed</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SCIENCE / Chemistry / Organic</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Asymmetric synthesis</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Synthese (chemie)</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Chiraliteit</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Enantiomeren</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Synthese asymetrique</subfield><subfield code="2">ram</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Composes organiques</subfield><subfield code="2">ram</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Asymmetric synthesis</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Asymmetrische Synthese</subfield><subfield code="0">(DE-588)4135603-2</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Asymmetrische Synthese</subfield><subfield code="0">(DE-588)4135603-2</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="8">1\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Aube, Jeffrey</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Druck-Ausgabe</subfield><subfield code="a">Gawley, Robert E.</subfield><subfield code="t">Principles of asymmetric synthesis</subfield><subfield code="b">1st ed</subfield><subfield code="d">Oxford, U.K. ; Tarrytown, N.Y. : Pergamon, 1996</subfield><subfield code="z">0080418767</subfield><subfield code="z">9780080418766</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-4-ENC</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-030729695</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">1\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield></record></collection> |
| id | DE-604.BV045342992 |
| illustrated | Illustrated |
| indexdate | 2024-07-10T08:15:28Z |
| institution | BVB |
| isbn | 9780080514772 0080514774 9780080418759 0080418759 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-030729695 |
| oclc_num | 316220611 |
| open_access_boolean | |
| physical | 1 online resource (xvii, 372 pages) illustrations |
| psigel | ZDB-4-ENC |
| publishDate | 1996 |
| publishDateSearch | 1996 |
| publishDateSort | 1996 |
| publisher | Pergamon |
| record_format | marc |
| series2 | Tetrahedron organic chemistry series |
| spelling | Gawley, Robert E. Verfasser aut Principles of asymmetric synthesis Robert E. Gawley and Jeffrey Aube 1st ed Oxford, U.K. ; Tarrytown, N.Y. Pergamon 1996 1 online resource (xvii, 372 pages) illustrations txt rdacontent c rdamedia cr rdacarrier Tetrahedron organic chemistry series v. 14 Print version record The world is chiral. Most of the molecules in it are chiral, and asymmetric synthesis is an important means by which enantiopure chiral molecules may be obtained for study and sale. Using examples from the literature of asymmetric synthesis (more than 1300 references), the aim of this book is to present a detailed analysis of the factors that govern stereoselectivity in organic reactions. It is important to note that the references were each individually checked by the authors to verify relevance to the topics under discussion. The study of stereoselectivity has evolved from issues of diastereoselectivity, through auxiliary-based methods for the synthesis of enantiomerically pure compounds (diastereoselectivity followed by separation and auxiliary cleavage), to asymmetric catalysis. In the latter instance, enantiomers (not diastereomers) are the products, and highly selective reactions and modern purification techniques allow preparation - in a single step - of chiral substances in 99% ee for many reaction types. After an explanation of the basic physical-organic principles of stereoselectivity, the authors provide a detailed, annotated glossary of stereochemical terms. A chapter on "Analytical Methods" provides a critical overview of the most common methods for analysis of stereoisomers. The authors then follow the 'tried-and-true' format of grouping the material by reaction type. Thus, there are four chapters on carbon-carbon bond forming reactions (enolate alkylations, organometal additions to carbonyls, aldol and Michael reactions, and cycloadditions and rearrangements), one chapter on reductions and hydroborations (carbon-hydrogen bond forming reactions), and one on oxidations (carbon-oxygen and carbon-nitrogen bond forming reactions). Leading references are provided to natural product synthesis that have been accomplished using a given reaction as a key step. In addition to tables of examples that show high selectivity, a transition state analysis is presented to explain - to the current level of understanding - the stereoselectivity of each reaction. In one case (Cram's rule) the evolution of the current theory is detailed from its first tentative (1952) postulate to the current Felkin-Anh-Heathcock formalism. For other reactions, only the currently accepted rationale is presented. Examination of these rationales also exposes the weaknesses of current theories, in that they cannot always explain the experimental observations. These shortcomings provide a challenge for future mechanistic investigations. An http://www.sciencedirect.com/science/publication?issn=14601567 & volume=14<HREF>http://asnetserver.as.miami.edu/rgawley/Book.html</HREF><HTXT>updated list of references</HTXT></URL> for this book can also be viewed SCIENCE / Chemistry / Organic bisacsh Asymmetric synthesis fast Synthese (chemie) gtt Chiraliteit gtt Enantiomeren gtt Synthese asymetrique ram Composes organiques ram Asymmetric synthesis Asymmetrische Synthese (DE-588)4135603-2 gnd rswk-swf Asymmetrische Synthese (DE-588)4135603-2 s 1\p DE-604 Aube, Jeffrey Sonstige oth Erscheint auch als Druck-Ausgabe Gawley, Robert E. Principles of asymmetric synthesis 1st ed Oxford, U.K. ; Tarrytown, N.Y. : Pergamon, 1996 0080418767 9780080418766 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Gawley, Robert E. Principles of asymmetric synthesis The world is chiral. Most of the molecules in it are chiral, and asymmetric synthesis is an important means by which enantiopure chiral molecules may be obtained for study and sale. Using examples from the literature of asymmetric synthesis (more than 1300 references), the aim of this book is to present a detailed analysis of the factors that govern stereoselectivity in organic reactions. It is important to note that the references were each individually checked by the authors to verify relevance to the topics under discussion. The study of stereoselectivity has evolved from issues of diastereoselectivity, through auxiliary-based methods for the synthesis of enantiomerically pure compounds (diastereoselectivity followed by separation and auxiliary cleavage), to asymmetric catalysis. In the latter instance, enantiomers (not diastereomers) are the products, and highly selective reactions and modern purification techniques allow preparation - in a single step - of chiral substances in 99% ee for many reaction types. After an explanation of the basic physical-organic principles of stereoselectivity, the authors provide a detailed, annotated glossary of stereochemical terms. A chapter on "Analytical Methods" provides a critical overview of the most common methods for analysis of stereoisomers. The authors then follow the 'tried-and-true' format of grouping the material by reaction type. Thus, there are four chapters on carbon-carbon bond forming reactions (enolate alkylations, organometal additions to carbonyls, aldol and Michael reactions, and cycloadditions and rearrangements), one chapter on reductions and hydroborations (carbon-hydrogen bond forming reactions), and one on oxidations (carbon-oxygen and carbon-nitrogen bond forming reactions). Leading references are provided to natural product synthesis that have been accomplished using a given reaction as a key step. In addition to tables of examples that show high selectivity, a transition state analysis is presented to explain - to the current level of understanding - the stereoselectivity of each reaction. In one case (Cram's rule) the evolution of the current theory is detailed from its first tentative (1952) postulate to the current Felkin-Anh-Heathcock formalism. For other reactions, only the currently accepted rationale is presented. Examination of these rationales also exposes the weaknesses of current theories, in that they cannot always explain the experimental observations. These shortcomings provide a challenge for future mechanistic investigations. An http://www.sciencedirect.com/science/publication?issn=14601567 & volume=14<HREF>http://asnetserver.as.miami.edu/rgawley/Book.html</HREF><HTXT>updated list of references</HTXT></URL> for this book can also be viewed SCIENCE / Chemistry / Organic bisacsh Asymmetric synthesis fast Synthese (chemie) gtt Chiraliteit gtt Enantiomeren gtt Synthese asymetrique ram Composes organiques ram Asymmetric synthesis Asymmetrische Synthese (DE-588)4135603-2 gnd |
| subject_GND | (DE-588)4135603-2 |
| title | Principles of asymmetric synthesis |
| title_auth | Principles of asymmetric synthesis |
| title_exact_search | Principles of asymmetric synthesis |
| title_full | Principles of asymmetric synthesis Robert E. Gawley and Jeffrey Aube |
| title_fullStr | Principles of asymmetric synthesis Robert E. Gawley and Jeffrey Aube |
| title_full_unstemmed | Principles of asymmetric synthesis Robert E. Gawley and Jeffrey Aube |
| title_short | Principles of asymmetric synthesis |
| title_sort | principles of asymmetric synthesis |
| topic | SCIENCE / Chemistry / Organic bisacsh Asymmetric synthesis fast Synthese (chemie) gtt Chiraliteit gtt Enantiomeren gtt Synthese asymetrique ram Composes organiques ram Asymmetric synthesis Asymmetrische Synthese (DE-588)4135603-2 gnd |
| topic_facet | SCIENCE / Chemistry / Organic Asymmetric synthesis Synthese (chemie) Chiraliteit Enantiomeren Synthese asymetrique Composes organiques Asymmetrische Synthese |
| work_keys_str_mv | AT gawleyroberte principlesofasymmetricsynthesis AT aubejeffrey principlesofasymmetricsynthesis |