Synthesis and reactions of [(allyloxy)methyl]sulfones - an equivalent for the [2,3]-wittig rearrangement of nonconjugated secondary carbanions-Reference-Cited by-同舟云学术

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Synthesis and reactions of [(allyloxy)methyl]sulfones - an equivalent for the [2,3]-wittig rearrangement of nonconjugated secondary carbanions

Published:1988-01 Issue:41 Volume:29 Page:5233-5236
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Brückner Reinhard,Peiseler Beate

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. A highly stereoselective synthesis of Z-trisubstituted olefins via [2,3]-sigmatropic rearrangement. Preference for a pseudoaxially substituted transition state

2. [2,3]-Wittig sigmatropic rearrangements in organic synthesis

3. Sulfenes by a ‘woff’-rearrangement of sulfonylcarbenes

4. p-TOLYLSULFONYLDIAZOMETHANE

5. α-Sulfonylether, 14. α-Monosubstituierte α-Sulfonylether – Synthesen und Eigenschaften

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1. Formation of Alcohols and Phenols by Ether Cleavage;Comprehensive Organic Transformations;2018-02-28

2. The Chemistry of Acyllithium Derivatives;PATAI'S Chemistry of Functional Groups;2009-12-15

3. Synthesis of 2-Arylcycloalka-2,4-dienones Using Sulfone-Based Methodology;The Journal of Organic Chemistry;2006-01-13

4. Diazomethylp-Tolyl Sulfone;Encyclopedia of Reagents for Organic Synthesis;2003-10-15

5. α-Oxy sulfones and sulfoximines: versatile intermediates;Journal of the Chemical Society, Perkin Transactions 1;2002-01-10

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