Author
C. Booma
Bio: C. Booma is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Lewis acids and bases & Lewis acid catalysis. The author has an hindex of 2, co-authored 2 publications receiving 50 citations.
Papers
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TL;DR: In this paper, a chiral pyrano[2,3-b] benzopyrans were synthesized by reaction of 2-C-acetoxymethylglycals 1 and 2 with phenols under Lewis acid catalysis.
37 citations
TL;DR: In this paper, the nucleophilic reaction of substituted 2-C-formylglycals with phenols under Lewis acid catalysis leading to 3C-arylhexoses is reported.
14 citations
Cited by
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TL;DR: Introduction 13103 CationicSequences 13104 Anionic Sequences 13106 3a.
339 citations
TL;DR: Asymmetric domino reactions are reviewed for the first time in this article, covering the classification and characteristics of these reactions together with the most important applications, showing that the concept of asymmetric Domino reactions has emerged as a powerful tool in asymmetric synthetic chemistry.
262 citations
TL;DR: An overview of all methodologies published during the last few years focused to the stereoselectives (diastereoselective or enantioselectIVE) synthesis of α-aminophosphonic acids and derivatives is reported.
244 citations
TL;DR: Glycals (or usually their O-substituted derivatives) are readily converted into 2,3-unsaturated glycosyl compounds with O-, C-, N-, S- or otherwise linked substituents at the anomeric position as discussed by the authors.
Abstract: Glycals (or usually their O-substituted derivatives) are readily converted into 2,3-unsaturated glycosyl compounds with O-, C-, N-, S- or otherwise linked substituents at the anomeric position. These products have been found to be useful for a range of synthetic purposes. In particular, the C-glycosidic compounds have served as readily available starting materials for the preparation of useful non-carbohydrate compounds. While these allylic rearrangement processes are usually conducted under the influence of Lewis acid catalysts, adaptations that involve activation of the allylic substituents of the starting glycals as leaving groups under neutral conditions have been developed. General features of the reactions are described as well as applications in synthesis and extensions of the basic processes.
146 citations
TL;DR: A review of recent developments in the use of promoters for the Ferrier rearrangement of O-, N-, C- and S-nucleophiles with glycals can be found in this paper.
121 citations