Cover of: Stereoselective synthesis | Robert S. Atkinson

Stereoselective synthesis

  • 529 Pages
  • 2.87 MB
  • 1757 Downloads
  • English
by
Wiley & Sons , Chichester [England], New York
Stereochemistry., Organic compounds -- Synth
StatementRobert S. Atkinson.
Classifications
LC ClassificationsQD481 .A79 1995
The Physical Object
Paginationxii, 529 p. :
ID Numbers
Open LibraryOL1096330M
ISBN 100471952508, 0471954195
LC Control Number94020918

This book provides a noteworthy compilation of the groundbreaking methods of stereoselective synthesis, belonging to the repertoire of every modern practitioner of synthetic organic chemistry. The general principles underlying these processes are highlighted as they form the basis for the rapid and continuing developments in the by: Stereoselective Synthesis is an invaluable aid not only to students in understanding this important area but also to those actively engaged in the syntheses of target molecules as single stereoisomers.

About the Author. Robert S. Atkinson is the author of Stereoselective Synthesis, published by Wiley. Reviews: 1. About this book The state-of-the-art in stereoselective synthesis. Thoroughly revised and updated, this enlarged second edition offers a plethora of valuable information on methods and reagents in stereoselective synthesis.

Written by a well-respected and experienced author, this textbook fills the gap for a concise introduction to the key concepts of organic stereochemistry and the most important classical and modern methods in stereoselective synthesis. The concepts are extensively illustrated in color, with practical examples and question-answer sets to help consolidate the Stereoselective synthesis book knowledge.

Jean Rodriguez is Professor and Director of the “Institut des Sciences Moléculaires de Marseille” at Aix-Marseille Université, with research interests including the development of new stereoselective domino Stereoselective synthesis book multicomponent reactions and their applications.

He was awarded the ACROS prize in Organic Chemistry () and the prize of the Division of Organic Chemistry (). A chemical reaction (or reaction @[email protected]) in which one or more new elements of @[email protected] are formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereoisomeric) products in unequal amounts.

Details Stereoselective synthesis FB2

Request PDF | Stereoselective Synthesis of a Novel Chiral Piperazine | (2S,6S)-2,4,6-Tris(phenylmethyl)piperazine was prepared in 11 steps and 53% overall. Book chapter Full text access Stereoselective Synthesis of Natural Products via Cationic and Radical Intermediates Shiroshi Shibuya, Tsutomu Yokomatsu, Yoko Yuasa.

In Stereoselective Synthesis expert authors present the best and most reliable methods available for the preparation of nonracemic compounds. These methods may be stoichiometric or catalytic, and the latter may include metal, organic, or enzyme catalysis. Stereoselective Synthesis of Tetrasubstituted Alkenes via Torquoselectivity-Controlled Olefination of Carbonyl Compounds with Ynolates W.-Y.

Siau Y. Zhang Y. Zhao Stereoselective Synthesis of Z-Alkenes. Hara.- Stereoselective Synthesis of Mono-fluoroalkenes.

De Paolis I. Chataigner J. Maddaluno Recent Advances in Stereoselective Synthesis. The stereoselective synthesis of different aldehydes of a hexahydropyrrolo[1,2-a]pyrazin-4(1H)-one scaffold for modular dipeptide mimetics such as has been reported Stereoselective synthesis book from enantiomerically pure azabicyclic alkenes These intermediates were diols and coupled with a second amino acid.

The product was cleaved at the level of the 1,2-diol with NaIO 4 to give aldehyde This book provides a noteworthy compilation of the groundbreaking methods of stereoselective synthesis, belonging to the repertoire of every modern practitioner of synthetic organic chemistry.

The general principles underlying these processes are highlighted as they form the basis for the rapid and continuing developments in the field. The work also features illustrative examples of drug and. (source: Nielsen Book Data) Summary Emphasizing synthetic strategy and practice, Stereoselective Synthesis of Drugs and Natural Products features experimental procedures for stereoselective synthetic reactions applicable to drug targets and natural products.

ISBN: OCLC Number: Description: xii, pages: illustrations ; 24 cm: Contents: 1. Selectivity in organic synthesis: stereochemical vocabulary Classification of stereochemical reactions used in this book Type 0 reactions: reactions in which no new chiral centres are created Type I reactions: those proceeding.

Devising methods and reagents for stereoselective synthesis is an intellectually demanding venture. Six experts on diastereo- and enantioselective synthesis contributed their papers to this volume.

They were presented at a symposium on stereoselective synthesis to honour Professor Dr. h.c. Rudolf Wiechert's achievements in medicinal. Stereoselective synthesis in organic chemistry.

New York: Springer-Verlag, © (OCoLC) Material Type: Internet resource: Document Type: Book, Internet Resource: All Authors / Contributors: Atta-ur- Rahman; Zahir Shah.

Stereoselective Synthesis of Z-Alkenes, by Woon-Yew Siau, Yao Zhang and Yu Zhao.- Stereoselective Synthesis of Mono-fluoroalkenes, by Shoji Hara.- Recent Advances in Stereoselective Synthesis of 1,3-Dienes, by Michael De Paolis, Isabelle Chataigner and Jacques Maddaluno   stereoselective synthesis 32 Stereoselective reactions: Stereoselective reactions 33 • Stereoselective reactions—reactions where one stereoisomer of product is formed predominantly because the reaction has a choice of pathways, and one pathway is more favourable than the other.

Stereoselective Synthesis in Organic Chemistry. Authors: Atta-ur-Rahman, Shah, Zahir Stereoselective Carbon-Carbon Bond Forming Reactions.

*immediately available upon purchase as print book shipments may be delayed due to the COVID crisis. ebook access is temporary and does not include ownership of the ebook.

Only valid for books Brand: Springer-Verlag New York. Highly Stereoselective First Synthesis of an A-Ring-Functionalized Bakkane: Novel Free-Radical Approach to 9-Acetoxyfukinanolide Olivier Hamelin, Jean-Pierre Deprés *, and Andrew E. Greene * Université Joseph Fourier, LEDSS, BP 53X Grenoble Cedex, FranceCited by: We report on the stereoselective synthesis of both molecular granny and square knots through the use of lanthanide-complexed overhand knots of specific handedness as three-crossing “entanglement synthons”.

The composite knots are assembled by combining two entanglement synthons (of the same chirality for a granny knot; of opposite handedness for a square knot) in three synthetic steps Cited by: 3.

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Book Series Help; Contact Portal SYNTHESIS Full-text search Catalyst- and Solvent-Free Synthesis of α-Amino Polyfluoroalkylphosphonates from Bis Stereoselective Total Synthesis of Arundinolides A and B Full Text HTML.

Written by a well-respected and experienced author, this textbook fills the gap for a concise introduction to the key concepts of organic stereochemistry and the most important classical and modern methods in stereoselective synthesis. The concepts are extensively illustrated in color, with practical examples and question-answer sets to help.

Figure 2. Importance of the chirality of the α‐aminophosphonic acids. In view of the different biological and chemical applications of the α‐aminophosphonic acids, nowadays the development of suitable synthetic methodologies for their preparation in optically pure form is a topic of great interest and many reviews have been recently published concerning their stereoselective synthesis [].Author: Mario Ordóñez, José Luis Viveros‐Ceballos, Iván Romero‐Estudillo.

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Book Description. This book offers an explanation of the specific ways that biocatalysis outperforms chemical catalysis by: utilizing ambient temperature and atmospheric pressure to minimize problems of isomerization, racemization, and epimerization; employing microbial cells and enzymes that can be immobilized and reused over many cycles; and overexpressing enzymes for greater economy and.

Find many great new & used options and get the best deals for Stereoselective Synthesis by M. Nogradi (, Hardcover) at the best online prices at eBay. Free shipping for many products. Stereochemistry and Stereoselective Synthesis. by Mihály Nógrádi,László Poppe,József Nagy,Gábor Hornyánszky,Zoltán Boros.

Share your thoughts Complete your review. Tell readers what you thought by rating and reviewing this book. Rate it * You Rated it *Brand: Wiley.

Stereoselective Alkene Synthesis. Topics in Current Chemistry (Book ) Share your thoughts Complete your review. Tell readers what you thought by rating and reviewing this book. Rate it * You Rated it *Brand: Springer Berlin Heidelberg. Further information about Stereoselective Synthesis (including sample pages and the table of contents) Category: Chemistry Carbonyl and imino groups are two of the most integral functional groups employed in organic synthesis.

stereoselective synthesis, this book features illustrative examples of drug and natural product syntheses, resulting in a rich source of stimulating ideas for the efficient use of asymmetric reactions in the users' own synthesis.

The authors adopt a novel approach in not attempting to present this. Stereoselective Synthesis by Carl P. Decicco,available at Book Depository with free delivery worldwide.In Science of Synthesis: Stereoselective Synthesis expert authors present the best and most reliable methods currently available for the preparation of nonracemic compounds.

These methods may be stoichiometric or catalytic, and the latter may include metal, organic, or enzyme catalysis. The three volumes of Stereoselective Synthesis provide an invaluable resource to the practicing synthetic. Stereoselective synthesis using hydantoinases and carbamoylases; aminoacidase-catalyzed preparation and further transformations of enantiopure alpha-hydrogen- and alpha,alpha-disubstitute alpha-amino acids; chemoenzymatic synthesis of pheromones, terpenes and other bioregulators; stereoselective biocatalysis for synthesis of some chiral pharmaceutical intermediates; .