Topics in stereochemistry

Topics in stereochemistry

by Eliel, Ernest L. Wilen, Samuel H.

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Computer Graphics and Molecular Modeling in the Analysis of Synthetic Targets (W. Ripka & J. Blaney). Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol Ethers (D. Oare & C. Heathcock). Conformational Analysis of Bicyclo [3.3.1] Nonanes and Their Hetero Analogs (N. Zefirov & V. Palyulin). Strained Olefins: Structure and Reactivity of Nonplanar Carbon-Carbon Double Bonds (W. Luef & R. Keese). Subject Index. Cumulative Author Index, Volumes 1-20. Cumulative Title Index, Volu…

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Title Statements

  • Full title :Topics in stereochemistry. / editors: Ernest L. Eliel, Samuel H. Wilen.

Summary

Computer Graphics and Molecular Modeling in the Analysis of Synthetic Targets (W. Ripka & J. Blaney). Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol Ethers (D. Oare & C. Heathcock). Conformational Analysis of Bicyclo [3.3.1] Nonanes and Their Hetero Analogs (N. Zefirov & V. Palyulin). Strained Olefins: Structure and Reactivity of Nonplanar Carbon-Carbon Double Bonds (W. Luef & R. Keese). Subject Index. Cumulative Author Index, Volumes 1-20. Cumulative Title Index, Volumes 1-20.

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Edition Statements

  • Publication Date:1991.

Publication Statements

  • Publisher(s):Wiley
  • Place of Publication:New York
  • Language:eng
  • Publication Date:1991.

The Physical Object

  • Description:1 online resource

Edition Identifiers

  • ISBN:9780470147290, 0470147296
  • oclc:ocn907033264
  • LC Classification:QD481
  • Dewey Decimal:547.1223

Table of Contents

TOPICS IN STEREOCHEMISTRY; CONTENTS; COMPUTER GRAPHICS AND MOLECULAR MODELING IN THE ANALYSIS OF SYNTHETIC TARGETS; ACYCLIC STEREOCONTROL IN MICHAEL ADDITION REACTIONS OF ENAMINES AND ENOL ETHERS; CONFORMATIONAL ANALYSIS OF BICYCLO[3.3.1]NONANES AND THEIR HETERO ANALOGS; STRAINED OLEFINS: STRUCTURE AND REACTIVITY OF NONPLANAR CARBON-CARBON DOUBLE BONDS; SUBJECT INDEX; CUMULATIVE AUTHOR INDEX, VOLUMES 1-20; CUMULATIVE TITLE INDEX, VOLUMES 1-20

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