Stereoselective synthesis of alcohols, L. Stereoselective synthesis of a C-15/C-27 segment of the venturicidines

DOI: 10.1002/jlac.199619961104

Source and publish data:

Liebigs Annalen p. 1717 - 1724 (1996)

Update date:2022-08-28

Topics:

Authors:

Hoffmann, Reinhard W.

Rolle, Ulrike

Goettlich, Richard

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Article abstract of DOI:10.1002/jlac.199619961104

Chain extension of an aldehyde by two "propionate" units has been attained by stereoselective allylboration with the chiral 1-methylbutenyl boronate 3 to give, e.g., the homoallylic alcohol 6, followed by a regioselective hydroboration/ carbonylation proc

Full text of DOI:10.1002/jlac.199619961104

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