The Synthesis of Alkenes via Reduction-Elimination of 1,2-Diol Cyclic Phosphate Derivatives-Reference-Cited by-同舟云学术

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The Synthesis of Alkenes via Reduction-Elimination of 1,2-Diol Cyclic Phosphate Derivatives

Published:1975-01 Issue:4 Volume:5 Page:293-297
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Marshall James A.,Lewellyn Morris E.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397917508064124

Reference6 articles.

1. Direct deoxygenation of vicinal diols with tungsten(IV). A new olefin synthesis

2. N,N,N',N'-Tetramethylphosphorodiamidate group. Useful function for the protection or reductive deoxygenation of alcohols and ketones

3. We are indebted to Professor Ireland for unpublished procedures detailing the preparation of various phosphoric esters

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1. The deoxydehydration (DODH) reaction: a versatile technology for accessing olefins from bio-based polyols;Green Chemistry;2020

2. N,N-Dimethyl Dichlorophosphoramide;Encyclopedia of Reagents for Organic Synthesis;2014-05-27

3. N,N-Dimethyl dichlorophosphoramide;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15

4. Preparation of Olefins;Compendium of Organic Synthetic Methods;2006-11-22

5. Synthesis of 2,3-Didehydro-2,3-dideoxynucleosides via Nucleoside Route.;Current Organic Synthesis;2006-08-01

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