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Journal ArticleDOI

Progress in the mitsunobu reaction. a review

David L. Hughes
- 01 Apr 1996 - 
- Vol. 28, Iss: 2, pp 127-164
TLDR
A review of progress in the MITSUNOBU this article reaction can be found in this article, with a focus on the MIT SUNOBU reaction and a review of the progress.
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This article is published in Organic Preparations and Procedures International.The article was published on 1996-04-01. It has received 373 citations till now. The article focuses on the topics: Mitsunobu reaction.

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The teraton challenge. A review of fixation and transformation of carbon dioxide

TL;DR: In this paper, the authors present a review of CO2, its synthetic reactions and their possible role in future CO2 mitigation schemes that have to match the scale of man-made CO2 in the atmosphere, which rapidly approaches 1 teraton.
Journal ArticleDOI

Mitsunobu and Related Reactions: Advances and Applications

TL;DR: This review concludes that Etherification without Cyclization and N-Alkylation should be considered as separate science, and the proposed treatment of Etherification with Cyclization as a separate science should be reconsidered.
Journal ArticleDOI

Aspects of carbon dioxide utilization

Iwao Omae
- 30 Jun 2006 - 
TL;DR: In this paper, the production of carbon dioxide with metal compounds as catalysts has been studied and further development of these production processes is expected, especially the productions of formic acids, formic acid methyl esters, formamides, methanol, dimethyl carbonate and urethanes with a dialkyltin catalyst.
References
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Journal ArticleDOI

Carbocyclic analogs of nucleosides. Part 2.. Synthesis of 2′,3′‐dideoxy‐5′‐homonucleoside analogs

TL;DR: A set of derivatives of cyclopentaneacetic acid cis-substituted at position 3 by nucleoside bases (both purines and pyrimidines) were prepared and characterized as mentioned in this paper.
Journal ArticleDOI

Palladium mediated allylic mitsunobu displacement: stereocontrolled synthesis of hepoxilin A3 and trioxilin A3 methyl esters

TL;DR: In this paper, a regio-and stereoselective palladium mediated allylic displacement under Mitsunobu conditions was exploited for the preparation of several hepoxilin A3 and trioxilin AA3 stereoisomers.
Journal ArticleDOI

The use of triphenylphosphine/diethyl azodicarboxylate (DEAD) for the cyclization of 1,4- and 1,5-amino alcohols

TL;DR: Application of the Mitsunobu reagent to the cyclization of 1,4 and 1,5 amino alcohols provided an assortment of azacycles in good yield as discussed by the authors.
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