Use of the Anomeric Allylation Reaction in Natural Products Synthesis - A Stereocontrolled Synthesis of Methyl Deoxypseudomonate B.

DOI: 10.1016/S0040-4039(01)81167-9

Source and publish data:

Tetrahedron Letters p. 2085 - 2088 (1984)

Update date:2022-08-03

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Authors:

Kozikowski, Alan P.

Sorgi, Kirk L.

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Article abstract of DOI:10.1016/S0040-4039(01)81167-9

L-lyxose has been elaborated to methyl deoxypseudomonate B (I) by a sequence of reactions involving the Lewis acid catalyzed anomeric allylation procedure and a stereospecific Grignard addition reaction.

Full text of DOI:10.1016/S0040-4039(01)81167-9

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