STEREOCONTROL OF A TERTIARY HYDROXYL GROUP VIA MICROBIAL EPOXIDATION. A FACILE SYNTHESIS OF PROSTAGLANDIN ω-CHAINS

DOI: 10.1016/S0040-4039(00)99526-1

Source and publish data:

Tetrahedron Letters p. 1583 - 1584 (1989)

Update date:2022-08-16

Topics:

Authors:

Takahashi, Osamu

Umezawa, Junko

Furuhashi, Keizo

Takagi, Motoyoshi

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Article abstract of DOI:10.1016/S0040-4039(00)99526-1

Optically active 1,2-epoxy-2-methylalkanes(1), useful precursors of tertiary alcohols, were prepared by microbial oxidation and converted to prostaglandin ω-chains.

Full text of DOI:10.1016/S0040-4039(00)99526-1

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