Olefination ofN-Sulfinylimines under Mild Conditions-Reference-Cited by-同舟云学术

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Olefination ofN-Sulfinylimines under Mild Conditions

Published:2017-02-24 Issue:8 Volume:2017 Page:1184-1190
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Dhara Shubhendu¹,Diesendruck Charles E.¹^ORCID

Affiliation:

1. Schulich Faculty of Chemistry; Technion - Israel Institute of Technology; 3200003 Haifa Israel

Funder

Technion-Israel Institute of Technology

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference88 articles.

1. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects

2. Synthesis of the 7-cis isomer of the natural leukotriene d4

3. Substituent effects and the Wittig mechanism: the case of stereospecific oxaphosphetane decomposition

4. Modification of the Wittig reaction to permit the stereospecific synthesis of certain trisubstituted olefins. Stereospecific synthesis of .alpha.-santalol

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1. Recent advances in synthesis of stilbene derivativesviacross-coupling reaction;Organic & Biomolecular Chemistry;2023

2. Direct Stereodivergent Olefination of Carbonyl Compounds with Sulfur Ylides;Journal of the American Chemical Society;2022-06-30

3. Aza-Peterson Olefinations: Rapid Synthesis of (E)-Alkenes;Synthesis;2021-04-28

4. Syntheses and Transformations of Sulfinamides;Synthesis;2021-03-11

5. Quinquevalent phosphorus acids;Organophosphorus Chemistry;2019

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