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Key chiral auxiliary applications /
Key Chiral Auxiliary Applications, Second Edition is a detailed compilation of chiral auxiliary applications organized by type of transformation. Continuing from the most important and relevant auxiliaries described in its predecessor, the three-volume set Compendium of Chiral Auxiliary Applications...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Waltham, MA :
Academic Press,
2014.
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| Edición: | Second edition. |
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
| LEADER | 00000cam a2200000 i 4500 | ||
|---|---|---|---|
| 001 | SCIDIR_ocn870333919 | ||
| 003 | OCoLC | ||
| 005 | 20231120111522.0 | ||
| 006 | m o d | ||
| 007 | cr cnu---unuuu | ||
| 008 | 140212s2014 mau o 000 0 eng d | ||
| 040 | |a OPELS |b eng |e rda |e pn |c OPELS |d E7B |d CDX |d OCLCF |d OCLCQ |d U3W |d D6H |d AU@ |d LQU |d S2H |d OCLCO |d OCLCQ |d OCLCO |d OCLCQ |d OCLCO | ||
| 019 | |a 1105173292 |a 1105561034 | ||
| 020 | |a 9780124170346 |q (electronic bk.) | ||
| 020 | |a 012417034X |q (electronic bk.) | ||
| 035 | |a (OCoLC)870333919 |z (OCoLC)1105173292 |z (OCoLC)1105561034 | ||
| 050 | 4 | |a QD262 | |
| 082 | 0 | 4 | |a 547.2 |2 23 |
| 100 | 1 | |a Roos, Gregory, |e author. | |
| 245 | 1 | 0 | |a Key chiral auxiliary applications / |c Gregory Roos, Murdoch University, Perth, Western Australia. |
| 250 | |a Second edition. | ||
| 264 | 1 | |a Waltham, MA : |b Academic Press, |c 2014. | |
| 264 | 4 | |c �2014 | |
| 300 | |a 1 online resource | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 520 | |a Key Chiral Auxiliary Applications, Second Edition is a detailed compilation of chiral auxiliary applications organized by type of transformation. Continuing from the most important and relevant auxiliaries described in its predecessor, the three-volume set Compendium of Chiral Auxiliary Applications (2001), as well as advances in the field, the book provides a vital and timely resource for chemists in the field. Each reaction class includes a series of tables and graphical abstracts of real reactions from the literature and patents to enable easy review and comparison of results. This anticipated edition is based on a screening of nearly 40,000 auxiliary reaction applications, with details supplied for the more than 13,000 selected representative entries: synthetic route, reagents, yields, diastereomeric/enantiomeric excesses, and characterization data. Updated and streamlined with more than 60% new material, Key Chiral Auxiliary Applications provides valuable guidance and reliable content for selecting the best auxiliary for a specific asymmetric synthetic transformation. Provides a comprehensive compilation based on nearly 40,000 diverse applications of chiral auxiliaries for selecting the best synthetic route to optically pure compoundsContains over 60% new material with 13,000+ auxiliary applications categorized by reaction type, with reaction details and chemical and optical yields in one unique resource. | ||
| 505 | 0 | |a 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. | |
| 505 | 8 | |a 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. | |
| 650 | 0 | |a Asymmetric synthesis. | |
| 650 | 0 | |a Enantioselective catalysis. | |
| 650 | 0 | |a Enantiomers. | |
| 650 | 6 | |a Synth�ese asym�etrique. |0 (CaQQLa)201-0242091 | |
| 650 | 6 | |a Catalyse �enantios�elective. |0 (CaQQLa)201-0353989 | |
| 650 | 6 | |a �Enantiom�eres. |0 (CaQQLa)201-0057866 | |
| 650 | 7 | |a Asymmetric synthesis |2 fast |0 (OCoLC)fst00819861 | |
| 650 | 7 | |a Enantiomers |2 fast |0 (OCoLC)fst00909487 | |
| 650 | 7 | |a Enantioselective catalysis |2 fast |0 (OCoLC)fst00909493 | |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780124170346 |z Texto completo |