Holdings: Asymmetric phase transfer catalysis

Asymmetric phase transfer catalysis:

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Bibliographic Details
Format:	Book
Language:	English
Published:	Weinheim WILEY-VCH 2008
Subjects:	Asymmetry (Chemistry) Phase-transfer catalysis Asymmetrische Reaktion Phasentransfer-Katalyse Patentschrift
Online Access:	Inhaltsverzeichnis http://deposit.dnb.de/cgi-bin/dokserv?id=3008909&prov=M&dok_var=1&dok_ext=htm Inhaltsverzeichnis
Physical Description:	XIV, 214 S. graph. Darst.
ISBN:	9783527318421 3527318429

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245	1	0	\|a Asymmetric phase transfer catalysis \|c ed. by Keiji Maruoka
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adam_text	* * * * * * * * * ******** XL LIST O F C O N T R I B U T O R S XLL1 T H E BASIC PRINCIPLE O F PHASE-TRANSFER CATALYSIS AND S O M E * M E C H A N I S T I C ASPECTS 1 * TAKUYA HASHIMOTO AND KEIJI MARUOKA 1.1* LNTRODUCTION 1* 1.2* INORGANIC BASE-PROMOTED ACTIVATION OF ACIDIC ORGANIC* COMPOUNDS 2* 1.2.1* GENERATION OF REACTIVE ONIUM CARBANION SPECIES 2* 1.2.2* STABILITY OF THE ONIUM CARBANION 3* 1.2.3* REACTIVITY OF THE ONIUM CARBANION 3* 1.2.4* NUCLUEOPHILIC SUBSTITUTION REACTION 4* 1.2.5* NUCLEOPHILIC ADDITION TO ELECTROPHILIC C=X DOUBLE BONDS 5* 1.3* PHASE-TRANSFER-CATALYZED ADDITION OF ANION SUPPLIED* AS METAL SALT 6* 1.4* USE OF CROWN ETHER AS PHASE-TRANSFER CATALYST 7* REFERENCES 7* 2 * C I N C H O N A - D E R I V E D CHIRAL PHASE-TRANSFER CATALYSTS FOR A M I N O * ACID SYNTHESIS 9* TAKASHI OOI 2.1* INTRODUCTION 9* 2.2* ET.-AMINO ACID SYNTHESIS 9* 2.2.1* MONOALKYLATION OF SCHIFF BASES DERIVED FROM GLYCINE 9* 2.2.2* ALKYLATION OF SCHIFF BASES DERIVED FROM ET.-ALKYL-ET.-AMINO* ACIDS 19* 2.2.3* OTHER ALKYLATIONS FOR ET.-AMINO ACID SYNTHESIS 21* 2.2.4* MICHAEL REACTION OF GLYCINATE BENZOPHENONE SCHIFF BASES 22* ASYMMETRIE PHASE TRANS}ER CATALYSIS. EDITED BY KEIJI MARUOKA COPYRIGHT 2008 WILEY-VCH VERLAG GMBH & CO. KGAA, WEINHEIM ISBN: 978-3-527-31842-1 VI I CONTENTS 2.2.5* ALDOL AND RELATED REAETIONS 24* 2.2.6* AZA-HENRY REAETION 25* 2.2.7* STRECKER REAETION 27* 2.2.8* AZIRIDINATION 27* 2.2.9* RADIEAL REAETION 28* 2.3* SS-AMINO ACID SYNTHESIS 29* 2.3.1* MANNICH REAETION 29* 2.3.2* CYCLOPROPANATION 29* 2.4* CONCLUSIONS 30* REFERENEES 31* 3* CINEHONA-DERIVED CHIRAJ PHASE-TRANSFER CATALYSTS FOR* OTHER ASYMMETRIE SYNTHESIS 35* SHIGERU ARAI 3.1* INTRODUETION 35* 3.2* ASYMMETRIE DARZENS REAETION 35* 3.3* ASYMMETRIE CONJUGATED ADDITION 36* 3.4* ASYMMETRIE ALDOL REAETION 39* 3.5* ASYMMETRIE OXYGEN-FUNETIONALIZATION 40* 3.6* ASYMMETRIE ALKYLATION 42* 3.7* ASYMMETRIE ALKENYLATION AND ALKYNYLATION 43* 3.8* ASYMMETRIE SN AROMATIE REAETION 45* 3.9* ASYMMETRIE STRECKER SYNTHESIS 46* 3.10* ASYMMETRIE FLUORINATION 46* REFERENEES 47* 4* CINEHONA-DERIVED CHIRAL POLY(PHASE-TRANSFER CATALYSTS)* FOR ASYMMETRIE SYNTHESIS 49* SANG-SUP JEW AND HYEUNG-GEUN PARK 4.1* CINCHONA ALKALOIDS 49* 4.1.1* CINCHONA ALKALOIDS IN ASYMMETRIE PHASE-TRANSFER CATALYSIS 49* 4.1.2* THE ORIGIN OF STEREOSELEETIVITY OF CINEHONA-PTCS 50* 4.2* DEVELOPMENT OF DIMERIE CINEHONA-PTCS BY THE PARK-JEW* GROUP 51* 4.2.1* DIMERIE CINEHONA-PTCS WITH PHENYL LINKER 51* 4.2.2* 1,3-DIMERIE CINEHONA-PTCS WITH ELEETRONIEALLY MODIFIED* PHENYL UNKER 56* 4.2.3* POLYMERIE CINEHONA-PTCS WITH OTHER LINKERS 56* 4.2.4* 1,3-PHENYL- AND 2,7-NAPHTHYL-LINKED DIMERIE CINEHONA-PTCS 57* 4.3* POLYMERIE PTCS DEVELOPED BY THE NAJERA GROUP 61* 4.4* POLYMERIE PTCS DEVELOPED BY THE SIVA GROUP 62* 4.5* POLYMERIE PTCS DEVELOPED BY THE WANG GROUP 63* 4.6* ASYMMETRIE EPOXIDATION WITH POLYMERIE CINEHONA-PTCS 63* 4.7* CONCLUSIONS 68* REFERENEES 68* 5 5.1 5.2 5.2.1 5.2.1.1 5.2.1.2 5.2.1.3 5.2.1.4 5.2.1.5 5.2.2 5.2.3 5.2.4 5.3 5.4 5.5 5.6 5.7 5.8 5.9 6* 6.1 6.2 6.3 6.4 6.5 6.6 6.7 6.7.1 6.7.2 6.7.3 6.8 6.9 6.10 6.10.1 CONTENTS IVII* BINAPHTHYL- AND BIPHENYL-MODIFIED CHIRAL PHASE-TRANSFER CATALYSTS* FOR ASYMMETRIE SYNTHESIS 71* KEIJI MARUOKA INTRODUETION 71* ALKYLATION 71* ASYMMETRIE SYNTHESIS OF CL-ALKYL CL-AMINO ACIDS AND THEIR* DERIVATIVES 71* ASYMMETRIE MONOALKYLATION OF GLYEINE ESTER SCHIFF BASES 71* ASYMMETRIE MONOALKYLATION OF GLYEINE AMIDE SCHIFF BASES 85* DIASTEREOSELEETIVE ALKYLATION OF GLYEINE SCHIFF BASE WITH* OPTIEALLY ENRIEHED ALKYL HALIDES 87* REEYCLABLE CATALYSTS AND REAGENTS AND SOLID-PHASE SYNTHESIS 87* APPLIEATION OF ASYMMETRIE SYNTHESIS OF CL-AMINO ACIDS 87* ASYMMETRIE SYNTHESIS OF CL,A-DIALKYL-CL-AMINO ACIDS 90* ALKYLATION OF SCHIFF BASE-AETIVATED PEPTIDES 94* OTHER ALKYLATIONS 97* MICHAEL ADDITION 99* ALDOL REAETION 105* MANNICH REAETION 106* NEBER REARRANGEMENT 106* EPOXIDATION 108* STRECKER REAETION 109* CONCLUSIONS 110* REFERENEES 111* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYSTS FOR ASYMMETRIE* SYNTHESIS 115* MASAKATSU SHIBASAKI AND TAKASHI OHSHIMA INTRODUCTION 115* SHORT SYNTHESES OF (+)-CYLINDRIEINE AND FORMAL SYNTHESIS OF* FORMAL SYNTHESIS OF (+)-CP-99,994 AND TOTAL SYNTHESIS OF* DESIGN AND SYNTHESIS OFTWO-CENTER CHIRAL PHASE-TRANSFER CATALYST 115* CATALYTIE ASYMMETRIE PHASE-TRANSFER ALKYLATION 118* CATALYTIE ASYMMETRIE PHASE-TRANSFER MICHAEL ADDITION TO* CL,SS-UNSATURATED ESTERS 119* CATALYTIE ASYMMETRIE PHASE-TRANSFER MICHAEL ADDITION TO ENONES 120* CATALYTIE ASYMMETRIE PHASE-TRANSFER MANNIEH-TYPE REAETION 122* SYNTHETIE APPLIEATIONS 123* ENANTIOSELEETIVE SYNTHESES OFAERUGINOSIN 298-A AND ITS ANALOGUES 123* (-)-LEPADIFORMINE 124* (+)-NEMONAPRIDE 125* CATALYST RECOVERY AND REUSE 126* ROLE OF TWO AMMONIUM CATIONS 127* OTHER TWO-CENTER CHIRAL PHASE-TRANSFER CATALYSTS 128* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM BINOL (1) 128* VIII I CONTENTS 6.10.2 6.10.3 6.10.4 6.10.5 6.11 7* 7.1 7.2 7.2.1 7.2.1.1 7.2.1.2 7.2.2 7.2.3 7.2.4 7.3 8* 8.1 8.2 8.2.1 8.2.2 8.2.3 8.3 8.4 8.5 8.5.1 8.5.2 8.5.3 8.5.4 8.6 TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM BINOL (2) 129* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM BINOL (3) 129* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM TARTRATE (1) 130* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM TARTRATE (2) 132* CONCLUSIONS 132* REFERENCES 133* OTHER CHIRAL PHASE-TRANSFER CATALYSTS FOR ASYMMETRIE* SYNTHESIS 135* HIROAKI SASAI AND MAHESH L. PATIL INTRODUCTION 135* OTHER CHIRAL PHASE-TRANSFER-CATALYZED REACTIONS 136* ALKYLATION 136* SUBSTRATE SCOPE 147* MECHANISTIC INVESTIGATIONS 149* MICHAEL REACTION 150* EPOXIDATION 152* HYDROXYLATION 156* CONCLUSIONS 157* REFERENCES 157* CROWN ETHERS, TADDOL, NOBIN AND METAL(SALEN) COMPLEXES* AS CHIRAL PHASE-TRANSFER CATALYSTS FOR ASYMMETRIE SYNTHESIS 161* MICHAEL NORTH INTRODUCTION 161* USE OFMETAL(SALEN) COMPLEXES AS CHIRAL PHASE-TRANSFER* USE OF OTHER METAL(SALEN) COMPLEXES AS CATALYSTS FOR ENOLATE* METAL(SALEN) COMPLEXES AS CATALYSTS FAR DARZENS* CROWN ETHERS AS CHIRAL PHASE-TRANSFER CATALYSTS 163* USE OF CROWN ETHERS IN ASYMMETRIE MICHAEL ADDITIONS 163* USE OF CROWN ETHERS IN DARZENS CONDENSATIONS 165* USE OF CROWN ETHERS IN ASYMMETRIE EPOXIDATIONS 166* USE OFTADDOLATES AS CHIRAL PHASE-TRANSFER CATALYSTS 166* USE OF NOBIN AND RELATED SPECIES AS ASYMMETRIE* PHASE-TRANSFER CATALYSTS 170* CATALYSTS 173* NICKEL(SALEN) COMPLEXES 173* COPPER(SALEN) COMPLEXES 175* ALKYLATION 182* CONDENSATIONS 183* CONCLUSIONS 184* REFERENCES 185* CONTENTS IIX* 9* CHIRAL QUATERNARY AMMONIUM FLUORIDES FOR ASYMMETRIE* SYNTHESIS 189* SEIJI SHIRAKAWA, TAKASHI GOI, AND KEIJI MARUOKA 9.1* INTRODUETION 189* 9.2* IN-SITU GENERATION OF CHIRAL QUATERNARY AMMONIUM* FLUORIDES 189* 9.3* CHIRAL QUATERNARY AMMONIUM FLUORIDES: PREPARATION AND* APPLIEATION TO ORGANOEATALYTIE ASYMMETRIE REAETIONS 193* 9.4* CHIRAL QUATERNARY AMMONIUM BIFLUORIDES: PREPARATION AND USE* AS ORGANOEATALYSTS FOR ASYMMETRIE CARBON-CARBON BOND-FORMING* REAETIONS 197* 9.5* CONCLUSIONS 205* REFERENEES 205* INDEX 207*
adam_txt	* * * * * * * * * ******** XL LIST O F C O N T R I B U T O R S XLL1 T H E BASIC PRINCIPLE O F PHASE-TRANSFER CATALYSIS AND S O M E * M E C H A N I S T I C ASPECTS 1 * TAKUYA HASHIMOTO AND KEIJI MARUOKA 1.1* LNTRODUCTION 1* 1.2* INORGANIC BASE-PROMOTED ACTIVATION OF ACIDIC ORGANIC* COMPOUNDS 2* 1.2.1* GENERATION OF REACTIVE ONIUM CARBANION SPECIES 2* 1.2.2* STABILITY OF THE ONIUM CARBANION 3* 1.2.3* REACTIVITY OF THE ONIUM CARBANION 3* 1.2.4* NUCLUEOPHILIC SUBSTITUTION REACTION 4* 1.2.5* NUCLEOPHILIC ADDITION TO ELECTROPHILIC C=X DOUBLE BONDS 5* 1.3* PHASE-TRANSFER-CATALYZED ADDITION OF ANION SUPPLIED* AS METAL SALT 6* 1.4* USE OF CROWN ETHER AS PHASE-TRANSFER CATALYST 7* REFERENCES 7* 2 * C I N C H O N A - D E R I V E D CHIRAL PHASE-TRANSFER CATALYSTS FOR A M I N O * ACID SYNTHESIS 9* TAKASHI OOI 2.1* INTRODUCTION 9* 2.2* ET.-AMINO ACID SYNTHESIS 9* 2.2.1* MONOALKYLATION OF SCHIFF BASES DERIVED FROM GLYCINE 9* 2.2.2* ALKYLATION OF SCHIFF BASES DERIVED FROM ET.-ALKYL-ET.-AMINO* ACIDS 19* 2.2.3* OTHER ALKYLATIONS FOR ET.-AMINO ACID SYNTHESIS 21* 2.2.4* MICHAEL REACTION OF GLYCINATE BENZOPHENONE SCHIFF BASES 22* ASYMMETRIE PHASE TRANS}ER CATALYSIS. EDITED BY KEIJI MARUOKA COPYRIGHT 2008 WILEY-VCH VERLAG GMBH & CO. KGAA, WEINHEIM ISBN: 978-3-527-31842-1 VI I CONTENTS 2.2.5* ALDOL AND RELATED REAETIONS 24* 2.2.6* AZA-HENRY REAETION 25* 2.2.7* STRECKER REAETION 27* 2.2.8* AZIRIDINATION 27* 2.2.9* RADIEAL REAETION 28* 2.3* SS-AMINO ACID SYNTHESIS 29* 2.3.1* MANNICH REAETION 29* 2.3.2* CYCLOPROPANATION 29* 2.4* CONCLUSIONS 30* REFERENEES 31* 3* CINEHONA-DERIVED CHIRAJ PHASE-TRANSFER CATALYSTS FOR* OTHER ASYMMETRIE SYNTHESIS 35* SHIGERU ARAI 3.1* INTRODUETION 35* 3.2* ASYMMETRIE DARZENS REAETION 35* 3.3* ASYMMETRIE CONJUGATED ADDITION 36* 3.4* ASYMMETRIE ALDOL REAETION 39* 3.5* ASYMMETRIE OXYGEN-FUNETIONALIZATION 40* 3.6* ASYMMETRIE ALKYLATION 42* 3.7* ASYMMETRIE ALKENYLATION AND ALKYNYLATION 43* 3.8* ASYMMETRIE SN AROMATIE REAETION 45* 3.9* ASYMMETRIE STRECKER SYNTHESIS 46* 3.10* ASYMMETRIE FLUORINATION 46* REFERENEES 47* 4* CINEHONA-DERIVED CHIRAL POLY(PHASE-TRANSFER CATALYSTS)* FOR ASYMMETRIE SYNTHESIS 49* SANG-SUP JEW AND HYEUNG-GEUN PARK 4.1* CINCHONA ALKALOIDS 49* 4.1.1* CINCHONA ALKALOIDS IN ASYMMETRIE PHASE-TRANSFER CATALYSIS 49* 4.1.2* THE ORIGIN OF STEREOSELEETIVITY OF CINEHONA-PTCS 50* 4.2* DEVELOPMENT OF DIMERIE CINEHONA-PTCS BY THE PARK-JEW* GROUP 51* 4.2.1* DIMERIE CINEHONA-PTCS WITH PHENYL LINKER 51* 4.2.2* 1,3-DIMERIE CINEHONA-PTCS WITH ELEETRONIEALLY MODIFIED* PHENYL UNKER 56* 4.2.3* POLYMERIE CINEHONA-PTCS WITH OTHER LINKERS 56* 4.2.4* 1,3-PHENYL- AND 2,7-NAPHTHYL-LINKED DIMERIE CINEHONA-PTCS 57* 4.3* POLYMERIE PTCS DEVELOPED BY THE NAJERA GROUP 61* 4.4* POLYMERIE PTCS DEVELOPED BY THE SIVA GROUP 62* 4.5* POLYMERIE PTCS DEVELOPED BY THE WANG GROUP 63* 4.6* ASYMMETRIE EPOXIDATION WITH POLYMERIE CINEHONA-PTCS 63* 4.7* CONCLUSIONS 68* REFERENEES 68* 5 5.1 5.2 5.2.1 5.2.1.1 5.2.1.2 5.2.1.3 5.2.1.4 5.2.1.5 5.2.2 5.2.3 5.2.4 5.3 5.4 5.5 5.6 5.7 5.8 5.9 6* 6.1 6.2 6.3 6.4 6.5 6.6 6.7 6.7.1 6.7.2 6.7.3 6.8 6.9 6.10 6.10.1 CONTENTS IVII* BINAPHTHYL- AND BIPHENYL-MODIFIED CHIRAL PHASE-TRANSFER CATALYSTS* FOR ASYMMETRIE SYNTHESIS 71* KEIJI MARUOKA INTRODUETION 71* ALKYLATION 71* ASYMMETRIE SYNTHESIS OF CL-ALKYL CL-AMINO ACIDS AND THEIR* DERIVATIVES 71* ASYMMETRIE MONOALKYLATION OF GLYEINE ESTER SCHIFF BASES 71* ASYMMETRIE MONOALKYLATION OF GLYEINE AMIDE SCHIFF BASES 85* DIASTEREOSELEETIVE ALKYLATION OF GLYEINE SCHIFF BASE WITH* OPTIEALLY ENRIEHED ALKYL HALIDES 87* REEYCLABLE CATALYSTS AND REAGENTS AND SOLID-PHASE SYNTHESIS 87* APPLIEATION OF ASYMMETRIE SYNTHESIS OF CL-AMINO ACIDS 87* ASYMMETRIE SYNTHESIS OF CL,A-DIALKYL-CL-AMINO ACIDS 90* ALKYLATION OF SCHIFF BASE-AETIVATED PEPTIDES 94* OTHER ALKYLATIONS 97* MICHAEL ADDITION 99* ALDOL REAETION 105* MANNICH REAETION 106* NEBER REARRANGEMENT 106* EPOXIDATION 108* STRECKER REAETION 109* CONCLUSIONS 110* REFERENEES 111* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYSTS FOR ASYMMETRIE* SYNTHESIS 115* MASAKATSU SHIBASAKI AND TAKASHI OHSHIMA INTRODUCTION 115* SHORT SYNTHESES OF (+)-CYLINDRIEINE AND FORMAL SYNTHESIS OF* FORMAL SYNTHESIS OF (+)-CP-99,994 AND TOTAL SYNTHESIS OF* DESIGN AND SYNTHESIS OFTWO-CENTER CHIRAL PHASE-TRANSFER CATALYST 115* CATALYTIE ASYMMETRIE PHASE-TRANSFER ALKYLATION 118* CATALYTIE ASYMMETRIE PHASE-TRANSFER MICHAEL ADDITION TO* CL,SS-UNSATURATED ESTERS 119* CATALYTIE ASYMMETRIE PHASE-TRANSFER MICHAEL ADDITION TO ENONES 120* CATALYTIE ASYMMETRIE PHASE-TRANSFER MANNIEH-TYPE REAETION 122* SYNTHETIE APPLIEATIONS 123* ENANTIOSELEETIVE SYNTHESES OFAERUGINOSIN 298-A AND ITS ANALOGUES 123* (-)-LEPADIFORMINE 124* (+)-NEMONAPRIDE 125* CATALYST RECOVERY AND REUSE 126* ROLE OF TWO AMMONIUM CATIONS 127* OTHER TWO-CENTER CHIRAL PHASE-TRANSFER CATALYSTS 128* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM BINOL (1) 128* VIII I CONTENTS 6.10.2 6.10.3 6.10.4 6.10.5 6.11 7* 7.1 7.2 7.2.1 7.2.1.1 7.2.1.2 7.2.2 7.2.3 7.2.4 7.3 8* 8.1 8.2 8.2.1 8.2.2 8.2.3 8.3 8.4 8.5 8.5.1 8.5.2 8.5.3 8.5.4 8.6 TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM BINOL (2) 129* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM BINOL (3) 129* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM TARTRATE (1) 130* TWO-CENTER CHIRAL PHASE-TRANSFER CATALYST DERIVED FROM TARTRATE (2) 132* CONCLUSIONS 132* REFERENCES 133* OTHER CHIRAL PHASE-TRANSFER CATALYSTS FOR ASYMMETRIE* SYNTHESIS 135* HIROAKI SASAI AND MAHESH L. PATIL INTRODUCTION 135* OTHER CHIRAL PHASE-TRANSFER-CATALYZED REACTIONS 136* ALKYLATION 136* SUBSTRATE SCOPE 147* MECHANISTIC INVESTIGATIONS 149* MICHAEL REACTION 150* EPOXIDATION 152* HYDROXYLATION 156* CONCLUSIONS 157* REFERENCES 157* CROWN ETHERS, TADDOL, NOBIN AND METAL(SALEN) COMPLEXES* AS CHIRAL PHASE-TRANSFER CATALYSTS FOR ASYMMETRIE SYNTHESIS 161* MICHAEL NORTH INTRODUCTION 161* USE OFMETAL(SALEN) COMPLEXES AS CHIRAL PHASE-TRANSFER* USE OF OTHER METAL(SALEN) COMPLEXES AS CATALYSTS FOR ENOLATE* METAL(SALEN) COMPLEXES AS CATALYSTS FAR DARZENS* CROWN ETHERS AS CHIRAL PHASE-TRANSFER CATALYSTS 163* USE OF CROWN ETHERS IN ASYMMETRIE MICHAEL ADDITIONS 163* USE OF CROWN ETHERS IN DARZENS CONDENSATIONS 165* USE OF CROWN ETHERS IN ASYMMETRIE EPOXIDATIONS 166* USE OFTADDOLATES AS CHIRAL PHASE-TRANSFER CATALYSTS 166* USE OF NOBIN AND RELATED SPECIES AS ASYMMETRIE* PHASE-TRANSFER CATALYSTS 170* CATALYSTS 173* NICKEL(SALEN) COMPLEXES 173* COPPER(SALEN) COMPLEXES 175* ALKYLATION 182* CONDENSATIONS 183* CONCLUSIONS 184* REFERENCES 185* CONTENTS IIX* 9* CHIRAL QUATERNARY AMMONIUM FLUORIDES FOR ASYMMETRIE* SYNTHESIS 189* SEIJI SHIRAKAWA, TAKASHI GOI, AND KEIJI MARUOKA 9.1* INTRODUETION 189* 9.2* IN-SITU GENERATION OF CHIRAL QUATERNARY AMMONIUM* FLUORIDES 189* 9.3* CHIRAL QUATERNARY AMMONIUM FLUORIDES: PREPARATION AND* APPLIEATION TO ORGANOEATALYTIE ASYMMETRIE REAETIONS 193* 9.4* CHIRAL QUATERNARY AMMONIUM BIFLUORIDES: PREPARATION AND USE* AS ORGANOEATALYSTS FOR ASYMMETRIE CARBON-CARBON BOND-FORMING* REAETIONS 197* 9.5* CONCLUSIONS 205* REFERENEES 205* INDEX 207*
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genre_facet	Patentschrift
id	DE-604.BV023029228
illustrated	Illustrated
index_date	2024-07-02T19:16:19Z
indexdate	2024-07-20T09:28:03Z
institution	BVB
isbn	9783527318421 3527318429
language	English
oai_aleph_id	oai:aleph.bib-bvb.de:BVB01-016233140
oclc_num	173721098
open_access_boolean
owner	DE-703 DE-19 DE-BY-UBM DE-83 DE-91G DE-BY-TUM DE-11 DE-29T
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physical	XIV, 214 S. graph. Darst.
publishDate	2008
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publisher	WILEY-VCH
record_format	marc
spelling	Asymmetric phase transfer catalysis ed. by Keiji Maruoka Weinheim WILEY-VCH 2008 XIV, 214 S. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Asymmetry (Chemistry) Phase-transfer catalysis Asymmetrische Reaktion (DE-588)4143270-8 gnd rswk-swf Phasentransfer-Katalyse (DE-588)4123947-7 gnd rswk-swf (DE-588)4173536-5 Patentschrift gnd-content Phasentransfer-Katalyse (DE-588)4123947-7 s Asymmetrische Reaktion (DE-588)4143270-8 s DE-604 Maruoka, Keiji Sonstige (DE-588)134042360 oth http://d-nb.info/98585152X/04 Inhaltsverzeichnis http://deposit.dnb.de/cgi-bin/dokserv?id=3008909&prov=M&dok_var=1&dok_ext=htm OEBV Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016233140&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle	Asymmetric phase transfer catalysis Asymmetry (Chemistry) Phase-transfer catalysis Asymmetrische Reaktion (DE-588)4143270-8 gnd Phasentransfer-Katalyse (DE-588)4123947-7 gnd
subject_GND	(DE-588)4143270-8 (DE-588)4123947-7 (DE-588)4173536-5
title	Asymmetric phase transfer catalysis
title_auth	Asymmetric phase transfer catalysis
title_exact_search	Asymmetric phase transfer catalysis
title_exact_search_txtP	Asymmetric phase transfer catalysis
title_full	Asymmetric phase transfer catalysis ed. by Keiji Maruoka
title_fullStr	Asymmetric phase transfer catalysis ed. by Keiji Maruoka
title_full_unstemmed	Asymmetric phase transfer catalysis ed. by Keiji Maruoka
title_short	Asymmetric phase transfer catalysis
title_sort	asymmetric phase transfer catalysis
topic	Asymmetry (Chemistry) Phase-transfer catalysis Asymmetrische Reaktion (DE-588)4143270-8 gnd Phasentransfer-Katalyse (DE-588)4123947-7 gnd
topic_facet	Asymmetry (Chemistry) Phase-transfer catalysis Asymmetrische Reaktion Phasentransfer-Katalyse Patentschrift
url	http://d-nb.info/98585152X/04 http://deposit.dnb.de/cgi-bin/dokserv?id=3008909&prov=M&dok_var=1&dok_ext=htm http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016233140&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
work_keys_str_mv	AT maruokakeiji asymmetricphasetransfercatalysis

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