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[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
Autore Coppola Gary M (Gary Mark), <1948->
Pubbl/distr/stampa Weinheim, : VCH, c1997
Descrizione fisica 1 online resource (x, 513 p. ) : ill. ;
Disciplina 547/.2
Altri autori (Persone) SchusterHerbert F <1949-> (Herbert Franz)
Soggetto topico Organic compounds - Synthesis
Alpha hydroxy acids
Enantiomers
Chemistry
Organic Chemistry
Physical Sciences & Mathematics
Soggetto genere / forma Electronic books
ISBN 1-280-55852-0
9786610558520
3-527-60085-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910146056903321
Coppola Gary M (Gary Mark), <1948->  
Weinheim, : VCH, c1997
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
Autore Coppola Gary M (Gary Mark), <1948->
Pubbl/distr/stampa Weinheim, : VCH, c1997
Descrizione fisica 1 online resource (x, 513 p. ) : ill. ;
Disciplina 547/.2
Altri autori (Persone) SchusterHerbert F <1949-> (Herbert Franz)
Soggetto topico Organic compounds - Synthesis
Alpha hydroxy acids
Enantiomers
Chemistry
Organic Chemistry
Physical Sciences & Mathematics
ISBN 1-280-55852-0
9786610558520
3-527-60085-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-996211425003316
Coppola Gary M (Gary Mark), <1948->  
Weinheim, : VCH, c1997
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
Autore Coppola Gary M (Gary Mark), <1948->
Pubbl/distr/stampa Weinheim, : VCH, c1997
Descrizione fisica 1 online resource (x, 513 p. ) : ill. ;
Disciplina 547/.2
Altri autori (Persone) SchusterHerbert F <1949-> (Herbert Franz)
Soggetto topico Organic compounds - Synthesis
Alpha hydroxy acids
Enantiomers
Chemistry
Organic Chemistry
Physical Sciences & Mathematics
ISBN 1-280-55852-0
9786610558520
3-527-60085-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910829816703321
Coppola Gary M (Gary Mark), <1948->  
Weinheim, : VCH, c1997
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
[Alpha]-hydroxy acids in enantioselective syntheses / / Gary M. Coppola, Herbert F. Schuster [[electronic resource]]
Autore Coppola Gary M (Gary Mark), <1948->
Pubbl/distr/stampa Weinheim, : VCH, c1997
Descrizione fisica 1 online resource (x, 513 p. ) : ill. ;
Disciplina 547/.2
Altri autori (Persone) SchusterHerbert F <1949-> (Herbert Franz)
Soggetto topico Organic compounds - Synthesis
Alpha hydroxy acids
Enantiomers
Chemistry
Organic Chemistry
Physical Sciences & Mathematics
ISBN 1-280-55852-0
9786610558520
3-527-60085-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910876654603321
Coppola Gary M (Gary Mark), <1948->  
Weinheim, : VCH, c1997
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Discrimination of mobile supramolecular chirality : acylative molecular transformations by organocatalysis / / Ayumi Imayoshi
Discrimination of mobile supramolecular chirality : acylative molecular transformations by organocatalysis / / Ayumi Imayoshi
Autore Imayoshi Ayumi
Pubbl/distr/stampa Singapore : , : Springer, , [2022]
Descrizione fisica 1 online resource (99 pages)
Disciplina 541.226
Collana Springer Theses
Soggetto topico Supramolecular chemistry
Chirality
Enantiomers
ISBN 981-16-7430-2
981-16-7431-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910743395103321
Imayoshi Ayumi  
Singapore : , : Springer, , [2022]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Key chiral auxiliary applications / / Gregory Roos
Key chiral auxiliary applications / / Gregory Roos
Autore Roos Gregory
Edizione [2nd ed.]
Pubbl/distr/stampa Waltham, [Massachusetts] ; ; Amsterdam, The Netherlands : , : Academic Press, , 2014
Descrizione fisica 1 online resource (1271 p.)
Disciplina 547
Soggetto topico Asymmetric synthesis
Enantioselective catalysis
Enantiomers
Soggetto genere / forma Electronic books.
ISBN 0-12-417115-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Front Cover; Key Chiral Auxiliary Applications; Copyright; CONTENTS; ACKNOWLEDGEMENTS; FOREWORD; PREFACE TO THE 2ND EDITION; ABBREVIATIONS; 1.INTRODUCTION; 1.1. BACKGROUND; 1.2. THE CHIRAL AUXILIARY APPROACH; 1.3. THIS COLLECTION; REFERENCES; 2.ALKYLATION AND RELATED REACTIONS I; 2.1 ALLYL AND BENZYL RELATED CARBANIONS; 2.2 ALLENIC ETHER TANDEM ACYLATION-CYCLIZATION; 2.3 ALDEHYDE DERIVED NUCLEOPHILES; 2.4 KETONE DERIVED NUCLEOPHILES; 2.5 ALDEHYDE AND KETONE ENOLATES WITH AUXILIARY-CONTAINING ELECTROPHILES; REFERENCES; 3.ALKYLATION AND RELATED REACTIONS II
3.1 α-ALKYLATION OF CARBOXYLIC ACID DERIVED NUCLEOPHILESREFERENCES; 4.ALKYLATION AND RELATED REACTIONS III; 4.1 α-ALKYLATION OF -HETEROATOM SUBSTITUTED ACID DERIVATIVES; 4.2 α-ALKYLATION OF CYCLIC CARBOXYLIC ACID DERIVATIVES; REFERENCES; 5.ALKYLATION AND RELATED REACTIONS IV; 5.3 α-HYDROXYLATION OF ACID DERIVATIVES; 5.1 α-ACYLATION OF ACID DERIVATIVES; 5.2 α-AMINATION OF ACYL DERIVATIVES; 5.4 α-SILYLATION, α-THIOLATION, AND α-SELENATION OF ACID DERIVATIVES; 5.5 α-HALOGENATION OF ACID DERIVATIVES; 5.6 REACTION OF PHOSPHORIC ACID DERIVATIVES WITH ELECTROPHILES
5.7 α-ALKYLATION OF SULFONIC ACID DERIVATIVES5.8 AROMATIC SUBSTITUTION; 5.9 NUCLEOPHILIC ALLYLIC SUBSTITUTION; 5.10 MISCELLANEOUS REACTIONS; REFERENCES; 6.ELECTROPHILIC RELATED ADDITION TO C=C; 6.1 REDUCTION AND RELATED REACTIONS; 6.2 ADDITION OF HALO-CONTAINING ADDENDS; 6.3 BISAMINATION; 6.4 ADDITION OF OXY-ADDENDS; 6.5 CYCLOPROPANATION; 6.6 CYCLOPROPENATION; 6.7 AZIRIDINATION; 6.8 ALKOXYSELENATION; 6.9 RADICAL ADDITION; REFERENCES; 7.CONJUGATE ADDITION I; 7.1 AUXILIARY ON DONOR NUCLEOPHILE - SIMPLE ADDITION; 7.2 AUXILIARY ON DONOR NUCLEOPHILE - TANDEM ADDITION; REFERENCES
8.CONJUGATE ADDITION II8.1 AUXILIARY ON ACCEPTOR α,β-UNSATURATED SYSTEM - SIMPLE ADDITION; REFERENCES; 9.CONJUGATE ADDITION III; 9.1 α,β-UNSATURATED ACYL DERIVATIVES - ADDITION OF HETERONUCLEOPHILES; 9.2 OTHER ACTIVATED SYSTEMS; 9.3 INTRAMOLECULAR REACTIONS; 9.4 AUXILIARY ON α,β-UNSATURATED SYSTEM - TANDEM ADDITION OFCARBON NUCLEOPHILES; 9.5 AUXILIARY ON ACCEPTOR α,β-UNSATURATED SYSTEM - TANDEM ADDITION OFHETERONUCLEOPHILES; 9.6 AUXILIARY ON ACCEPTOR α,β-UNSATURATED SYSTEM - RADICAL ADDITION; 9.7 NUCLEOPHILIC ADDITION TO TRANSITION-METAL ALKENE/ARENE COMPLEXES; REFERENCES
10.ADDITION TO C=N BONDS10.1 REDUCTION OF IMINES, IMINIUM IONS, HYDRAZONES AND OXIMES; 10.2 NUCLEOPHILIC ADDITION; 10.3 RADICAL ADDITION; 10.4 UGI COUPLING; REFERENCES; 11.ADDITION TO C=O BONDS I; 11.1 REDUCTION; 11.2 WITTIG & RELATED OLEFINATION; 11.3 ADDITION OF ORGANOMETALLIC AND RELATED REAGENTS; REFERENCES; 12.ADDITION TO C=O BONDS II; 12.1 ADDITION OF ENOLATES (ALDOL AND RELATED REACTIONS); REFERENCES; 13.ADDITION TO C=O BONDS III; 13.1 ADDITION OF ENOLATES (ALDOL AND RELATED REACTIONS); 13.2 TANDEM REACTIONS; 13.3 RADICAL REACTIONS; REFERENCES; 14. CYCLOADDITIONS I
14.1 [2+2]-CYCLOADDITIONS
Record Nr. UNISA-996426337703316
Roos Gregory  
Waltham, [Massachusetts] ; ; Amsterdam, The Netherlands : , : Academic Press, , 2014
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui