The stereochemistry of the 1,4-elimination of thiocyanic acid from hex-3-ene-2,5-diyl dithiocyanates-Reference-Cited by-同舟云学术

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The stereochemistry of the 1,4-elimination of thiocyanic acid from hex-3-ene-2,5-diyl dithiocyanates

Published:1993 Issue:3 Volume: Page:246
ISSN:0022-4936
Container-title:Journal of the Chemical Society, Chemical Communications
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Schoepfer Joseph,Eichenberger Eugen,Neier Reinhard

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930000246

Cited by 9 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 2-Cyano-2-siloxyvinylallenes via Cyanide-Induced Brook Rearrangement in γ-Bromo-α,β,γ,δ-unsaturated Acylsilanes;The Journal of Organic Chemistry;2014-12-08

2. ChemInform Abstract: The Stereochemistry of the 1,4-Elimination of Thiocyanic Acid from Hex- 3-ene-2,5-diyl Dithiocyanates.;ChemInform;2010-08-20

3. Highly Stereoselective Approach to Alk-2-yne-1,4-diols by Oxazaborolidine-Mediated Reduction of Alk-2-yne-1,4-diones;The Journal of Organic Chemistry;2004-07-03

4. Amino-Claisen rearrangements and Diels-Alder reactions of ketene N,O-acetals: Reactivity studies. On the way to a novel tandem process?;Helvetica Chimica Acta;2000-10-04

5. Application of the Novel Tandem Process Diels-Alder Reaction/Ireland-Claisen Rearrangement to the Synthesis of rac-Juvabione and rac-Epijuvabione;Helvetica Chimica Acta;2000-09-06

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