Journal ArticleDOI
Progress in the mitsunobu reaction. a review
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.About:
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.read more
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
Key green chemistry research areas—a perspective from pharmaceutical manufacturers
David J. C. Constable,Peter J. Dunn,John D. Hayler,Guy R. Humphrey,Johnnie L. Leazer,Russell J. Linderman,Kurt T. Lorenz,Julie B. Manley,Bruce A. Pearlman,Andrew S. Wells,Aleksey Zaks,Tony Y. Zhang +11 more
TL;DR: An assessment of the current state of the art in green chemistry and green engineering areas and to highlight areas for future improvement are provided.
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
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
Mitsunobu reactions of glycals with phenoxide nucleophiles are SN2′-selective
Aditya Sobti,Gary A. Sulikowski +1 more
TL;DR: The C3-hydoxyl group of l-rhamnal (4) and d-glucal 7 underwent SN2′-selective Mitsunobu displacements with substituted phenoxide nucleophiles as discussed by the authors.
Journal ArticleDOI
Synthesis of a chiral α-(aminooxy)arylacetic ester. II. A route through a chiral 2-hydroxy-2-phenylacetic acid derivative
Hisao Iwagami,Masanobu Yatagai,Masakazu Nakazawa,Haruo Orita,Yutaka Honda,Takashi Ohnuki,Toshihide Yukawa +6 more
TL;DR: In this paper, a simple and practical synthetic route was developed for the synthesis of a chiral α-(aminooxy) ester (S)-16, which is a synthetic intermediate for a potent antipseudomonal cephalosporin antibiotic M-14659.
Journal ArticleDOI
Mitsunobu reaction of 1,5-anhydro-3,4,6-tri-O-benzyl-2-deoxy-2-hydroxymethyl-hex-1-enitols and 1,5-anhydro-2-deoxy-4,6-O-protected-hex-1-enitols. A novel method for the synthesis of 2-C-methylene glycosides and an useful alternative to Ferrier rearrangement
TL;DR: In this paper, a simple and convenient method for the synthesis of aryl-3,4,6-tri-O-benzyl-2-deoxy-methylene-hexopyranosides 5,6 and 7, glycosides which are not accessible by the conventional Ferrier rearrangement, has been described based on the Mitsunobu reaction of alcohols 3 and 4 with substituted phenols.
Journal ArticleDOI
An epimer of 5'-noraristeromycin and its antiviral properties.
Suhaib M. Siddiqi,Xing Chen,Stewart W. Schneller,Satoru Ikeda,Robert Snoeck,Graciela Andrei,Jan Balzarini,Erik De Clercq +7 more
TL;DR: The results of this study suggest that (-)-3 should be pursued for the treatment of those virus infections [that is, pox (VV), rhabdo (VSV), paramyxo (parainfluenza), and reo] that appear to be exquisitively sensitive to the compound.
Journal ArticleDOI
Direct synthesis of N-protected chiral amino acids from imidodicarbonates employing either Mitsunobu or triflate alkylation. Feasibility study using lactate with particular reference to 15N-labelling
TL;DR: In this article, two approaches to N,N-diprotected chiral α-amino acid esters, based on selected imidodi-carbonates as amine synthons, have been explored.
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The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium Salts
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