Secondary and tertiary alcohols as nucleophiles in the stereospecific synthesis of substituted tetrahydrofurans by cyclisation of 1,3-diols with phenylsulfanyl migration-Reference-Cited by-同舟云学术

Secondary and tertiary alcohols as nucleophiles in the stereospecific synthesis of substituted tetrahydrofurans by cyclisation of 1,3-diols with phenylsulfanyl migration

Published:1996-06 Issue:23 Volume:37 Page:4077-4080
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Eames Jason,de las Heras Maria A.,Warren Stuart

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. Electrostatic modulation of hydroxyl group ionization in acidic media. Evidence for the competitive operation of intramolecular SN2 reactions

2. .gamma.-Lithioalkoxides via reductive lithiation of oxetanes by aromatic radical-anions

3. Hydroxypropylation

4. Acid-catalyzed cyclization of 1,4-diols tethered to (butadiene)iron tricarbonyl segments. Isotopic labeling as a mechanistic probe of stereochemical retention during tetrahydrofuran formation

5. 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

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1. Enantioselective organocatalyzed functionalization of benzothiophene and thiophenecarbaldehyde derivatives;Tetrahedron;2012-06

2. ChemInform Abstract: Secondary and Tertiary Alcohols as Nucleophiles in the Stereospecific Synhesis of Substituted Tetrahydrofurans by Cyclization of 1,3-Diols with Phenylsulfanyl Migration.;ChemInform;2010-08-04

3. Iodine-Catalyzed Synthesis of Five-Membered Cyclic Ethers from 1,3-Diols under Solvent-Free Conditions;Journal of Oleo Science;2009

4. An Efficient Synthesis of Five-membered Cyclic Ethers from 1,3-Diols Using Molecular Iodine as a Catalyst;Journal of Oleo Science;2008

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