Synthesis of C-glycosyl compounds: the reaction of acetylated glycals with tert-butoxycarbonylmethylzinc bromide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference32 articles.
1. Stereoselectivity in the electrophile-promoted cyclizations of a hydroxyolefin derived from arabinose. Synthesis of a phosphonate isostere of β-(=D)-arabinose-1, 5-diphosphate
2. Synthesis of phosphonate analogs of α-d-glucopyranosyl and α-d-galactopyranosyl phosphate
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1. One-pot Mukaiyama type carbon-Ferrier rearrangement of glycals: Application in the synthesis of chromanone 3-C-glycosides;Carbohydrate Research;2017-01
2. Synthesis and Cytotoxicity of 2,3-Enopyranosyl C-Linked Conjugates of Genistein;Molecules;2014-05-30
3. Zinc mediated activation of terminal alkynes: stereoselective synthesis of alkynyl glycosides;Org. Biomol. Chem.;2014
4. The carbon-Ferrier rearrangement: an approach towards the synthesis of C-glycosides;Arkivoc;2013-01-10
5. ChemInform Abstract: Synthesis of C-Glycosyl Compounds: The Reaction of Acetylated Glycals with tert-Butoxycarbonylmethylzinc Bromide.;ChemInform;2010-08-18
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