Tether-Mediated Stereocontrol in Intramolecular Azomethine Ylide Cycloadditions

The computationally guided design of a silicon-based tether system for stereoselective intramolecular azomethine ylide cycloadditions is described.

Saved in:
Bibliographic Details
Published inJournal of organic chemistry Vol. 59; no. 22; pp. 6510 - 6511
Main Authors Garner, Philip P, Cox, Philip B, Klippenstein, Stephen J, Youngs, Wiley J, McConville, David B
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 01.11.1994
Amer Chemical Soc
Subjects
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
ASYMMETRIC APPROACH
4+2 CYCLOADDITIONS
QUINOCARCIN
DIELS-ALDER REACTIONS
Online AccessGet full text

Cover

More Information
Summary:The computationally guided design of a silicon-based tether system for stereoselective intramolecular azomethine ylide cycloadditions is described.
Bibliography:istex:A9E035C4AECAD0C719EC0205D4B0B939E53A5A00
ark:/67375/TPS-80HFJ8C3-W
ISSN:0022-3263
1520-6904
DOI:10.1021/jo00101a005