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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

The mechanism of the Mitsunobu azide modification and the effect of additives on the rate of hydroxyl group activation.

TL;DR: In this paper, the Mitsunobu azide modification has been studied by NMR using a hindered alcohol and the principle intermediates involved have been tentatively identifiably identified.
Journal ArticleDOI

Synthesis of Some Purine Carbocyclic Isosteres of 2′,3′-Dideoxy-3′-C-Hydroxymethyl Nucleosides as Potential Inhibitors of HIV

TL;DR: In this paper, the synthesis of enantiomerically pure carbocyclic 2′, 3′-dideoxy-3′-C-hydroxymethyl derivatives of adenine, inosine and guanine is described.
Journal ArticleDOI

Synthesis of nucleosides by direct replacement of the anomeric hydroxy-group

TL;DR: In this paper, a purine nucleosides of aldoses and ketoses were synthesized by treatment of an appropriately protected sugar derivative having a free anomeric hydroxy-group with 6-chloropurine, diethyl azodicarboxylate, and methyldiphenylphosphine.
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