Synthesis of two rigid diacylglycerol analogues having a bis-butyrolactone skeleton

DOI: 10.1016/S0040-4039(00)91668-X

Source and publish data:

Tetrahedron Letters p. 1539 - 1542 (1992)

Update date:2022-08-03

Topics:

Authors:

Lee, Jeewoo

Teng, Kelly

Marquez, Victor E.

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Article abstract of DOI:10.1016/S0040-4039(00)91668-X

The stereoselective synthesis of two rigid diacylglycerol analogues starting from protected D-apio-L-furanose (apiose) is described. The construction of the desired bis-butyrolactone bicyclic structure was accomplished via an intramolecular radical cycliz

Full text of DOI:10.1016/S0040-4039(00)91668-X

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