An Efficient Route to Hydroxy-1-alkenyl Phenyl Sulfides by an Eliminative Ring-Cleavage Reaction-Reference-Cited by-同舟云学术

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An Efficient Route to Hydroxy-1-alkenyl Phenyl Sulfides by an Eliminative Ring-Cleavage Reaction

Published:1992 Issue:08 Volume:1992 Page:668-670
ISSN:0936-5214
Container-title:Synlett
language:en
Short-container-title:Synlett

Author:

Takano Seiichi,Sugihara Yoshiaki,Ogasawara Kunio

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1992-21452.pdf

Cited by 11 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. Formation of Alkenes by Elimination;Comprehensive Organic Transformations;2018-02-28

2. From Silylated Trishomoallylic Alcohols to Dioxaspiroundecanes or Oxocanes: Catalyst and Substitution Influence;The Journal of Organic Chemistry;2016-03-14

3. ChemInform Abstract: An Efficient Route to Hydroxy-1-alkenyl Phenyl Sulfides by an Eliminative Ring-Cleavage Reaction.;ChemInform;2010-08-20

4. Optically active 2,3-epoxy sulfides as precursors to 3-hydroxy-1,2-dithioethers and 3-hydroxy-1-alkenylthioethers;Tetrahedron Letters;1999-09

5. Lewis acid induced rearrangement of 2,3-epoxy sulfides; regiospecific trapping of thiiranium ion intermediates with nitrogen heterocycles and amides. Use of imines as nucleophilic equivalents for the selective monoalkylation of primary amines;Tetrahedron;1996-03

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