Total asymmetric synthesis of 3-amino-3-deoxy-L-talose and derivatives

DOI: 10.1016/0008-6215(94)80034-0

Source and publish data:

Carbohydrate Research p. 175 - 187 (1994)

Update date:2022-08-02

Topics: Derivatives Optically active Experimental terms Chiral compound Total asymmetric synthesis

Authors:

Hunenberger

Allemann

Vogel Vogel

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Article abstract of DOI:10.1016/0008-6215(94)80034-0

(1R,2R,4R)-2-exo-Cyano-7-oxabicyclo[2.2.1]hept-5-en-2-yl (1S')-camphanate [(+)-1, Diels-Alder adduct of furan to 1-cyanovinyl (1S)-camphanate] was transformed with high stereoselectivity into (1R,2R,6R,7R)-4-phenyl-3,10-dioxa-5-azatricyclo[5.2.1.0^2,6

Full text of DOI:10.1016/0008-6215(94)80034-0

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Product name:methyl 3-amino-1,5-anhydro-2-O,3-N-benzoyl-3-deoxy-α-L-talofuranuronate

Cas No:157506-31-5

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