Efficient Conversion of Vicinal Diols to Alkenes by Treatment of the Corresponding Dimesylates with a Catalytic, Minimally Fluorous, Recoverable Diaryl Diselenide and Sodium Borohydride-Reference-Cited by-同舟云学术

Efficient Conversion of Vicinal Diols to Alkenes by Treatment of the Corresponding Dimesylates with a Catalytic, Minimally Fluorous, Recoverable Diaryl Diselenide and Sodium Borohydride

Published:2000-11-11 Issue:25 Volume:2 Page:4029-4031
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Crich David¹,Neelamkavil Santhosh¹,Sartillo-Piscil Fernando¹

Affiliation:

1. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061, and Unidad de Investigación en Síntesis Orgánica, Facultad de Ciencias Químicas, Universidad Autónoma de Puebla, Puebla, México

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0066532

Reference13 articles.

1. Synthesis of 2‘,3‘-Didehydro-2‘,3‘-dideoxynucleosides by Reaction of 5‘-Protected Nucleoside 2‘,3‘-Dimesylates with Telluride Dianion: A General Route from Cis Vicinal Diols to Olefins

2. Synthesis of 2‘,3‘-Didehydro-2‘,3‘-dideoxynucleosides by Reaction of 5‘-O-Protected Nucleoside 2‘,3‘-Dimesylates with Lithium Areneselenolates

3. Inhibition of Stannane-Mediated Radical Rearrangements by a Recoverable, Minimally Fluorous Selenol

4. Design, synthesis, application and recovery of a minimally fluorous diaryl diselenide for the catalysis of stannane-mediated radical chain reactions

5. Efficient One-Pot Conversion of Carbonyl Compounds to Their α,β-Unsaturated Derivatives Using a Recoverable, Minimally Fluorous Organoselenium Reagent

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