Scope and limitation of the [1,4] SPh shift in the synthesis of allylic alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Sulfur participation in solvolysis involving four-membered ring intermediates
2. Rearrangements of phenylthio substituted 1,n-diols with toluene-p-sulfonic acid and with toluene-p-sulfonyl chloride
3. Transformation of cyclic α-phenylthio aldehydes by stereoselective aldol reactions and phenylthio migration into spirocyclic lactones and ethers, and E-allylic alcohols with 1,4-related chiral centres
4. Endocyclic vs. exocyclic attack in nucleophilic displacement reactions on five- and six-membered cyclic onium salts
5. Stereo- and regio-chemical control in phenylthio migration around rings of sizes 5–15
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1. From (Phenylsulfanyl)cycloalkanecarbaldehydes to Optically Active Spirocyclic Tetrahydrofurans: Stereospecific Resolution of Symmetric Aldehydes through (S)-Proline-Catalysed Aldol Reaction;European Journal of Organic Chemistry;2014-09-19
2. ChemInform Abstract: Scope and Limitation of the (1,4) SPh Shift in the Synthesis of Allylic Alcohols.;ChemInform;2010-08-05
3. Controlling neighbouring group participation from thioacetals;Tetrahedron Letters;2003-03
4. Stereochemically controlled synthesis of substituted 1,2-oxathianes;Journal of the Chemical Society, Perkin Transactions 1;2002-09-23
5. The stereoselective synthesis of oxetanes; exploration of a new, Mitsunobu-style procedure for the cyclisation of 1,3-diols;Journal of the Chemical Society, Perkin Transactions 1;2001-10-30
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