Literature DB >> 21483986

Facile synthesis of unusual glycosyl carbamates and amino acid glycosides from propargyl 1,2-orthoesters as glycosyl donors.

Ashif Y Shaikh1, Gopalsamy Sureshkumar, Debasish Pati, Sayam Sen Gupta, Srinivas Hotha.   

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.

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Year:  2011        PMID: 21483986     DOI: 10.1039/c1ob05056g

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

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3.  Gold-catalyzed glycosidation for the synthesis of trisaccharides by applying the armed-disarmed strategy.

Authors:  Abhijeet K Kayastha; Srinivas Hotha
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4.  p-Nitrophenyl carbonate promoted ring-opening reactions of DBU and DBN affording lactam carbamates.

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  4 in total

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