A new synthetic route to chiral, multiply functionalized cyclopentane rings

DOI: 10.1016/S0040-4039(00)79149-0

Source and publish data:

Tetrahedron Letters p. 5261 - 5264 (1992)

Update date:2022-07-30

Topics:

Authors:

Contelles

Ruiz Ruiz

Sanchez Sanchez

Jimeno Jimeno

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Article abstract of DOI:10.1016/S0040-4039(00)79149-0

The tribyltin hydride mediated free radical cyclization of sugar derivatives 4-6 gives the annulated furanose 9-11 in good yield and high diastereoselectivity. This protocol is a new synthetic route for the preparation of complex cyclopentanoid molecules.

Full text of DOI:10.1016/S0040-4039(00)79149-0

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