Inverse Klemer-Rodemeyer Fragmentation. Application to the Synthesis of Positional Isomers of Ristosamine and Acosamine

DOI: 10.1246/cl.1986.1055

Source and publish data:

Chemistry Letters p. 1055 - 1056 (1986)

Update date:2022-08-03

Topics:: Authors:

Morin, Christophe

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Article abstract of DOI:10.1246/cl.1986.1055

Application of the Klemer-Rodemeyer fragmentation to a 4-O-silicon substituted rhamnose benzylidene acetal leads to "inverse opening" of the dioxolane ring, thus opening a new route to 2-amino-2,3,6-trideoxy-L-hexoses.

Full text of DOI:10.1246/cl.1986.1055

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Inverse Klemer-Rodemeyer Fragmentation. Application to the Synthesis of Positional Isomers of Ristosamine and Acosamine

DOI: 10.1246/cl.1986.1055

Source and publish data:

Authors:

Article abstract of DOI:10.1246/cl.1986.1055

Full text of DOI:10.1246/cl.1986.1055

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