New route to (Z)-allylic sulfides via a 10-membered thiolcarbonate.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/37/9/37_9_2567/_pdf
Cited by 7 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. Development of New Synthetic Reactions Using Hetero-Heavy Atoms and Their Application to Synthesis of Biofunctional Molecules;Chemical and Pharmaceutical Bulletin;2020-01-01
2. A new method for synthesis of S-aryl-O-alkyl thiolcarbonates: selenium-catalyzed reaction of alcohols with carbon monoxide and diaryl disulfides;Tetrahedron Letters;2005-10
3. [3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 9. total synthesis of (±)-yellow scale pheromone via 10-membered thiolcarbonate;Tetrahedron;1993-08
4. [3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 5. Stereoselective synthesis of the yellow scale pheromone;Tetrahedron Letters;1992-04
5. [3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 8. highly stereoselective synthesis of (Z- or (E)-double bonds by controlling chairlike-boatlike transition states in the [3,3]sigmatropic rearrangement of 8-membered thionocarbonates;Tetrahedron;1992-01
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