Stereodefined Access to 3‐Deoxy Sugars Through a Tandem Baylis–Hillman and Lewis Acid Catalyzed Reaction Sequence | Zendy

Radha Krishna Palakodety | Zendy; Manjuvani Applashetti | Zendy; Narsingam Mogili | Zendy; Raju Galla | Zendy

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Stereodefined Access to 3‐Deoxy Sugars Through a Tandem Baylis–Hillman and Lewis Acid Catalyzed Reaction Sequence

Author(s) -

Radha Krishna Palakodety,

Manjuvani Applashetti,

Narsingam Mogili,

Raju Galla

Publication year - 2010

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200901109

Subject(s) - chemistry , adduct , lewis acids and bases , tandem , baylis–hillman reaction , catalysis , sequence (biology) , stereochemistry , sugar , organic chemistry , combinatorial chemistry , biochemistry , materials science , composite material

An innovative synthetic protocol is reported for the ready access to 3‐deoxy sugars in both D and L forms as exclusive products (des >95 %) in high yields through a stereodefined Lewis acid catalyzed reaction sequence of the sugar‐derived Baylis–Hillman adducts.

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