Total synthesis of an anticancer agent, mucocin. 1. Stereoselective synthesis of the left-half segment

DOI: 10.1016/S0040-4039(98)02439-3

Source and publish data:

Tetrahedron Letters p. 723 - 726 (1999)

Update date:2022-08-03

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Authors:

Takahashi, Shunya

Nakata, Tadashi

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Article abstract of DOI:10.1016/S0040-4039(98)02439-3

The left-half segment of mucocin (1) was stereoselectively synthesized through a coupling reaction of a tetrahydropyranyl aldehyde and a tetrahydrofuran derivative having an ethynyl group, which were prepared from 2,3,4,6-tetra-O-benzyl-D-galactono-1,5-la

Full text of DOI:10.1016/S0040-4039(98)02439-3

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