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Org Biomol Chem ; 9(17): 5951-9, 2011 Sep 07.
Article in English | MEDLINE | ID: mdl-21483986

ABSTRACT

Propargyl 1,2-O-orthoesters are exploited for the synthesis of 1,2-trans O-glycosides of protected amino acids. N-Fmoc- and N-Cbz protected serine/threonine - benzyl/methyl esters reacted well with glucosyl-, galactosyl-, mannosyl- and lactosyl- derived propargyl 1,2-orthoesters affording respective 1,2-trans glycosides in good yields under AuBr(3)/4 Å MS Powder/CH(2)Cl(2)/rt. t-Boc serine derivative gave serine 1,2-orthoester and glycosyl carbamate. Optimized conditions enabled preparation of new glycosyl carbamates from N-Boc protected amines in a single step using gold catalysts and propargyl 1,2-orthoesters in excellent yields.


Subject(s)
Amino Acids/chemical synthesis , Carbamates/chemical synthesis , Glycosides/chemical synthesis , Amino Acids/chemistry , Carbamates/chemistry , Esters/chemical synthesis , Esters/chemistry , Glycosides/chemistry
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