Enzymatic single-step formation of laureat in and its key intermediate, prelaureatin, from (3Z, 6S, 7S)-laurediol

DOI: 10.1016/0040-4039(92)88128-R

Source and publish data:

Tetrahedron Letters p. 2017 - 2018 (1992)

Update date:2022-07-29

Topics:

Authors:

Fukuzawa, Akio

Takasugi, Yasunori

Murai, Akio

Nakamura, Masao

Tamura, Mamoru

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Article abstract of DOI:10.1016/0040-4039(92)88128-R

A bicyclic natural bromo ether, laureatin (7), and its monocyclic key intermediate, prelaureatin (6), have enzymatically been transformed from their original precursor, (3Z, 6S, 7S)-laurediol in single-step by lactoperoxidase.

Full text of DOI:10.1016/0040-4039(92)88128-R

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Product name:2H-Oxocin-3-ol,8-[(1S)-1-bromopropyl]-3,4,7,8-tetrahydro-2-(2Z)-2-penten-4-yn-1-yl-,(2S,3S,8R)-

Cas No:139610-22-3

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