Stereoelectronic Control in Diels−Alder Reaction of Dissymmetric 1,3-Dienes
The Diels−Alder reaction is a widely employed protocol in which four stereogenic centers are generated in a predictable manner with olefin geometry, adjoining chiral center, and transition-state topology serving as the main controlling elements. However, when the Diels−Alder partners are in a dissym...
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Published in | Accounts of chemical research Vol. 33; no. 5; pp. 278 - 286 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
01.05.2000
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Subjects | |
Online Access | Get full text |
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