Stereoselective Synthesis

Stereoselective Synthesis by Mihaly Nogradi Download PDF EPUB FB2

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 readers 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 and 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.

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 starting 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.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.