Experimental evidence for the lack of stereoselectivity in the electrophilic quench of .alpha.-sulfonyl carbanions
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00299a028
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Studies on synthesis of spirolactone annulated bicyclo[2.2.2]octanes: tricyclic core of yaoshanenolides;Tetrahedron;2014-08
2. 3.03 Alkylation of α-Sulfur-Containing Carbanions;Comprehensive Organic Synthesis II;2014
3. The Ring Opening of Oxabicyclic Compounds Controlled by a Phenylsulfonyl Group. Synthetic Applications.;Current Organic Chemistry;2002-06-01
4. Experimental Evidence for Negative Hyperconjugation as a Component of the Polar Effect: Variation of the Ease of α-Sulfonyl Carbanion Formation with the Orientation of a β-Alkoxy Substituent;Journal of the American Chemical Society;2000-10-01
5. Sulfonyl-Stabilized Allylic Norbornenyl and Norbornyl Carbanions: Structure and Stereoselectivity of Reaction with Electrophiles;European Journal of Organic Chemistry;1999-07
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