Stereoselective Heterocycle Synthesis via Alkene Difunctionalization: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation
Saved in:
| Main Author: | |
|---|---|
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Cham
Springer International Publishing
2018
Cham Springer |
| Edition: | 1st ed. 2018 |
| Series: | Springer Theses, Recognizing Outstanding Ph.D. Research
|
| Subjects: | |
| Online Access: | BTU01 TUM01 Volltext |
| Physical Description: | 1 Online-Ressource (XXIX, 365 p. 167 illus., 12 illus. in color) |
| ISBN: | 9783319775074 |
| ISSN: | 2190-5053 |
| DOI: | 10.1007/978-3-319-77507-4 |
Staff View
MARC
| LEADER | 00000nmm a2200000zcb4500 | ||
|---|---|---|---|
| 001 | BV046062045 | ||
| 003 | DE-604 | ||
| 005 | 00000000000000.0 | ||
| 007 | cr|uuu---uuuuu | ||
| 008 | 190724s2018 |||| o||u| ||||||eng d | ||
| 020 | |a 9783319775074 |c Online |9 978-3-319-77507-4 | ||
| 024 | 7 | |a 10.1007/978-3-319-77507-4 |2 doi | |
| 035 | |a (ZDB-2-CMS)9783319775074 | ||
| 035 | |a (OCoLC)1111904169 | ||
| 035 | |a (DE-599)BVBBV046062045 | ||
| 040 | |a DE-604 |b ger |e rda | ||
| 041 | 0 | |a eng | |
| 049 | |a DE-634 |a DE-91 | ||
| 082 | 0 | |a 547.05 |2 23 | |
| 084 | |a CHE 000 |2 stub | ||
| 100 | 1 | |a Petrone, David A. |e Verfasser |4 aut | |
| 245 | 1 | 0 | |a Stereoselective Heterocycle Synthesis via Alkene Difunctionalization |b Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation |c by David A. Petrone |
| 250 | |a 1st ed. 2018 | ||
| 264 | 1 | |a Cham |b Springer International Publishing |c 2018 | |
| 264 | 1 | |a Cham |b Springer | |
| 300 | |a 1 Online-Ressource (XXIX, 365 p. 167 illus., 12 illus. in color) | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b c |2 rdamedia | ||
| 338 | |b cr |2 rdacarrier | ||
| 490 | 0 | |a Springer Theses, Recognizing Outstanding Ph.D. Research |x 2190-5053 | |
| 650 | 4 | |a Organometallic Chemistry | |
| 650 | 4 | |a Catalysis | |
| 650 | 4 | |a Medicinal Chemistry | |
| 650 | 4 | |a Chemistry, Organic | |
| 650 | 4 | |a Catalysis | |
| 650 | 4 | |a Biochemistry | |
| 776 | 0 | 8 | |i Erscheint auch als |n Druck-Ausgabe |z 978-3-319-77506-7 |
| 776 | 0 | 8 | |i Erscheint auch als |n Druck-Ausgabe |z 978-3-319-77508-1 |
| 776 | 0 | 8 | |i Erscheint auch als |n Druck-Ausgabe |z 978-3-030-08472-1 |
| 856 | 4 | 0 | |u https://doi.org/10.1007/978-3-319-77507-4 |x Verlag |z URL des Erstveröffentlichers |3 Volltext |
| 912 | |a ZDB-2-CMS | ||
| 940 | 1 | |q ZDB-2-CMS_2018_Fremddaten | |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-031443360 | ||
| 966 | e | |u https://doi.org/10.1007/978-3-319-77507-4 |l BTU01 |p ZDB-2-CMS |x Verlag |3 Volltext | |
| 966 | e | |u https://doi.org/10.1007/978-3-319-77507-4 |l TUM01 |p ZDB-2-CMS |x Verlag |3 Volltext | |
Record in the Search Index
| _version_ | 1804180338672402432 |
|---|---|
| any_adam_object | |
| author | Petrone, David A. |
| author_facet | Petrone, David A. |
| author_role | aut |
| author_sort | Petrone, David A. |
| author_variant | d a p da dap |
| building | Verbundindex |
| bvnumber | BV046062045 |
| classification_tum | CHE 000 |
| collection | ZDB-2-CMS |
| ctrlnum | (ZDB-2-CMS)9783319775074 (OCoLC)1111904169 (DE-599)BVBBV046062045 |
| dewey-full | 547.05 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547.05 |
| dewey-search | 547.05 |
| dewey-sort | 3547.05 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie Chemie |
| doi_str_mv | 10.1007/978-3-319-77507-4 |
| edition | 1st ed. 2018 |
| format | Electronic eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01978nmm a2200505zcb4500</leader><controlfield tag="001">BV046062045</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">190724s2018 |||| o||u| ||||||eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9783319775074</subfield><subfield code="c">Online</subfield><subfield code="9">978-3-319-77507-4</subfield></datafield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/978-3-319-77507-4</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ZDB-2-CMS)9783319775074</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)1111904169</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV046062045</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="049" ind1=" " ind2=" "><subfield code="a">DE-634</subfield><subfield code="a">DE-91</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">547.05</subfield><subfield code="2">23</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">CHE 000</subfield><subfield code="2">stub</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Petrone, David A.</subfield><subfield code="e">Verfasser</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Stereoselective Heterocycle Synthesis via Alkene Difunctionalization</subfield><subfield code="b">Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation</subfield><subfield code="c">by David A. Petrone</subfield></datafield><datafield tag="250" ind1=" " ind2=" "><subfield code="a">1st ed. 2018</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Cham</subfield><subfield code="b">Springer International Publishing</subfield><subfield code="c">2018</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Cham</subfield><subfield code="b">Springer</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource (XXIX, 365 p. 167 illus., 12 illus. in color)</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">Springer Theses, Recognizing Outstanding Ph.D. Research</subfield><subfield code="x">2190-5053</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Organometallic Chemistry</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Catalysis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Medicinal Chemistry</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemistry, Organic</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Catalysis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Biochemistry</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Druck-Ausgabe</subfield><subfield code="z">978-3-319-77506-7</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Druck-Ausgabe</subfield><subfield code="z">978-3-319-77508-1</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Erscheint auch als</subfield><subfield code="n">Druck-Ausgabe</subfield><subfield code="z">978-3-030-08472-1</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1007/978-3-319-77507-4</subfield><subfield code="x">Verlag</subfield><subfield code="z">URL des Erstveröffentlichers</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-2-CMS</subfield></datafield><datafield tag="940" ind1="1" ind2=" "><subfield code="q">ZDB-2-CMS_2018_Fremddaten</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-031443360</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1007/978-3-319-77507-4</subfield><subfield code="l">BTU01</subfield><subfield code="p">ZDB-2-CMS</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">https://doi.org/10.1007/978-3-319-77507-4</subfield><subfield code="l">TUM01</subfield><subfield code="p">ZDB-2-CMS</subfield><subfield code="x">Verlag</subfield><subfield code="3">Volltext</subfield></datafield></record></collection> |
| id | DE-604.BV046062045 |
| illustrated | Not Illustrated |
| indexdate | 2024-07-10T08:34:11Z |
| institution | BVB |
| isbn | 9783319775074 |
| issn | 2190-5053 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-031443360 |
| oclc_num | 1111904169 |
| open_access_boolean | |
| owner | DE-634 DE-91 DE-BY-TUM |
| owner_facet | DE-634 DE-91 DE-BY-TUM |
| physical | 1 Online-Ressource (XXIX, 365 p. 167 illus., 12 illus. in color) |
| psigel | ZDB-2-CMS ZDB-2-CMS_2018_Fremddaten |
| publishDate | 2018 |
| publishDateSearch | 2018 |
| publishDateSort | 2018 |
| publisher | Springer International Publishing Springer |
| record_format | marc |
| series2 | Springer Theses, Recognizing Outstanding Ph.D. Research |
| spelling | Petrone, David A. Verfasser aut Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation by David A. Petrone 1st ed. 2018 Cham Springer International Publishing 2018 Cham Springer 1 Online-Ressource (XXIX, 365 p. 167 illus., 12 illus. in color) txt rdacontent c rdamedia cr rdacarrier Springer Theses, Recognizing Outstanding Ph.D. Research 2190-5053 Organometallic Chemistry Catalysis Medicinal Chemistry Chemistry, Organic Biochemistry Erscheint auch als Druck-Ausgabe 978-3-319-77506-7 Erscheint auch als Druck-Ausgabe 978-3-319-77508-1 Erscheint auch als Druck-Ausgabe 978-3-030-08472-1 https://doi.org/10.1007/978-3-319-77507-4 Verlag URL des Erstveröffentlichers Volltext |
| spellingShingle | Petrone, David A. Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation Organometallic Chemistry Catalysis Medicinal Chemistry Chemistry, Organic Biochemistry |
| title | Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation |
| title_auth | Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation |
| title_exact_search | Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation |
| title_full | Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation by David A. Petrone |
| title_fullStr | Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation by David A. Petrone |
| title_full_unstemmed | Stereoselective Heterocycle Synthesis via Alkene Difunctionalization Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation by David A. Petrone |
| title_short | Stereoselective Heterocycle Synthesis via Alkene Difunctionalization |
| title_sort | stereoselective heterocycle synthesis via alkene difunctionalization bulky phosphine ligands enable pd catalyzed arylhalogenation arylcyanation and diarylation |
| title_sub | Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation |
| topic | Organometallic Chemistry Catalysis Medicinal Chemistry Chemistry, Organic Biochemistry |
| topic_facet | Organometallic Chemistry Catalysis Medicinal Chemistry Chemistry, Organic Biochemistry |
| url | https://doi.org/10.1007/978-3-319-77507-4 |
| work_keys_str_mv | AT petronedavida stereoselectiveheterocyclesynthesisviaalkenedifunctionalizationbulkyphosphineligandsenablepdcatalyzedarylhalogenationarylcyanationanddiarylation |