ChemInform Abstract: Regioselective Alkylation and Acylation of Methyl 2,6‐Dideoxyhexopyranosides via Their Stannylene Acetals: Key Step for the Synthesis of Daunosamine and Related Amino Sugars.

C Monneret,J.‐C Florent,R Gagnet

doi:10.1002/chin.198751329

ChemInform Abstract: Regioselective Alkylation and Acylation of Methyl 2,6‐Dideoxyhexopyranosides via Their Stannylene Acetals: Key Step for the Synthesis of Daunosamine and Related Amino Sugars.

C Monneret, J.‐C Florent + Show 1 more

https://doi.org/10.1002/chin.198751329

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Journal: ChemInform

Publication Date: Dec 22, 1987

Affiliation: Délégation Paris 5, French National Centre for Scientific Research

#Acylation Of Methyl #Stannylene Acetals #Regioselective Alkylation #Benzyl Ether #Alkylation Of Methyl #Regioselective Acylation #Amino Sugars

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AbstractThe L‐lyxo‐hexopyranoside (III) is converted into the benzyl ether (I) and the tosylate (V).

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ChemInform Abstract: Regioselective Alkylation and Acylation of Methyl 2,6‐Dideoxyhexopyranosides via Their Stannylene Acetals: Key Step for the Synthesis of Daunosamine and Related Amino Sugars.