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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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Citations
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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

A convenient preparation of alkyl nitriles by the mitsunobu procedure

TL;DR: In this paper, a convenient preparation of alkyl nitriles from alcohols extending the use of the Mitsunobu reaction is described, and a method for extracting alkyls from alcohol is described.
Journal ArticleDOI

Novel biopolymers for drug discovery.

TL;DR: The solid phase synthesis and generation of libraries of “unnatural biopolymers” is described, characterized by novel backbones and building blocks, the properties of which may modify their pharmacological and folding properties.
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Enantiomerically pure amino alcohols and diamino alcohols from l-aspartic acid. application to the synthesis of epi- and diepislaframine

TL;DR: In this paper, a method for the synthesis of enantiomerically pure 3-amino alcohols including 3,4-diamino derivatives is described starting from natural aspartic acid.
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Stereospecific dehydrative alkylation of bis-sulfones: synthesis of a lesser tea tortrix pheromone

TL;DR: The intra-and intermolecular condensation of alcohols with bis-sulfone methylenes, i.e., dehydrative alkylation, using DEAD and Ph 3 P Proceeds stereospecifiically at room temperature under essentially neutral conditions affording good yield of alkyl/ annulation products as discussed by the authors.
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N2-Isobutyryl-O6-[2-(p-Nitrophenyl)Ethyl]Guanine: A New Building Block for the Efficient Synthesis of Carbocyclic Guanosine Analogs

TL;DR: In this paper, the synthesis of different types of carbocyclic analogs of guanosine in high yield under Mitsunobu conditions is described. But only the desired N9-substituted derivatives of guanine are formed.
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