Palladium(0)-Catalyzed Enantioselective O,S-Rearrangement of Racemic O-Allylic Thiocarbamates: A New Entry to Enantioenriched Allylic Sulfur Compounds-Reference-Cited by-同舟云学术

Palladium(0)-Catalyzed Enantioselective O,S-Rearrangement of Racemic O-Allylic Thiocarbamates: A New Entry to Enantioenriched Allylic Sulfur Compounds

Published:2002-01-18 Issue:4 Volume:67 Page:1153-1161
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gais Hans-Joachim¹,Böhme Achim¹

Affiliation:

1. Institut für Organische Chemie der Rheinisch-Westfälischen Technischen Hochschule Aachen, Professor-Pirlet-Strasse 1, D-52056 Aachen, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010668b

Reference52 articles.

1. Stereospecificity and stereoselectivity in the [3,2] sigmatropic rearrangement of open chain sulphonium ylides

2. Enantioselective syntheses of organosulfur compounds via [2,3] sigmatropic rearrangements of ylides derived from di(allyl), di(propargyl), and di(benzyl) sulfide complexes; Control of carbon configuration by an easily resolved and recycled rhenium auxiliary

3. Metal-catalyzed ylide formation and [2,3] sigmatropic rearrangement of allyl sulfides with trimethylsilyldiazomethane

4. [2,3]-Sigmatropic rearrangement of allylic sulfur ylides derived from trimethylsilyldiazomethane (TMSD)

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