O
Oleg A. Zubkov
Researcher at Victoria University of Wellington
Publications - 5
Citations - 102
Oleg A. Zubkov is an academic researcher from Victoria University of Wellington. The author has contributed to research in topics: Allylic rearrangement & Nucleophilic substitution. The author has an hindex of 3, co-authored 5 publications receiving 99 citations.
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Transformation of Glycals into 2,3‐Unsaturated Glycosyl Derivatives
Robert J. Ferrier,Oleg A. Zubkov +1 more
TL;DR: Various elimination procedures conducted on appropriate pyranoid and furanoid carbohydrate derivatives, especially on O-protected glycosyl halides afford cyclic vinyl ethers which Fischer (inappropriately) named glycals, form the major part of this chapter.
Journal ArticleDOI
A simple synthesis of 8-(methoxycarbonyl)octyl 3,6-di-O-(α-d-mannopyranosyl)-α-d-mannopyranoside and derivatives and their use in the preparation of neoglycoconjugates
TL;DR: In this article, 8-(Methoxycarbonyl) octyl 3,6-di- O -(α- d -mannopyranosyl)-α-d -mannoside (10) was synthesized in 54% yield by regioselective diglycosylation of unprotected mannoside 4, employing the trichloroacetimidate donor 1, followed by debenzoylation.
Journal ArticleDOI
Novel Anti-Inflammatory Spongian Diterpenes from the New Zealand Marine Sponge Chelonaplysilla violacea
TL;DR: In this article, six rearranged spongian diterpenes were isolated from the New Zealand sponge Chelonaplysilla violacea and the structures of the six metabolites were determined by extensive spectral analysis.
Journal ArticleDOI
Transformation of Glycals into 2,3‐Unsaturated Glycosyl Derivatives
Robert J. Ferrier,Oleg A. Zubkov +1 more
TL;DR: Glycosyl halides are used extensively in general organic synthesis and for the preparation of non-carbohydrate natural products as well as biologically important complex carbohydrates and glycoconjugates as discussed by the authors.
Journal ArticleDOI
A Simple Synthesis of 8-(Methoxycarbonyl)octyl 3,6-Di-O-(α-D-mannopyranosyl)-α-D-mannopyranoside and Derivatives and Their Use in the Preparation of Neoglycoconjugates.
TL;DR: In this paper, 8-(Methoxycarbonyl) octyl 3,6-di- O -(α- d -mannopyranosyl)-α-d -mannoside (10) was synthesized in 54% yield by regioselective diglycosylation of unprotected mannoside 4, employing the trichloroacetimidate donor 1, followed by debenzoylation.