Synthetic studies on concanamycin A: Synthesis of the C5~C13 and C20~C28 segments

DOI: 10.1016/S0040-4039(98)01233-7

Source and publish data:

Tetrahedron Letters p. 6003 - 6006 (1998)

Update date:2022-07-31

Topics:

Authors:

Jyojima, Takaaki

Katohno, Masataka

Miyamoto, Naoki

Nakata, Masaya

Matsumura, Shuichi

Toshima, Kazunobu

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Article abstract of DOI:10.1016/S0040-4039(98)01233-7

The enantioselective synthesis of the C5~C13 (2) and C20~C28 (3) segments, which are promising synthetic intermediates toward the total synthesis of the 18-membered macrolide antibiotic, concanamycin A (1), were described.

Full text of DOI:10.1016/S0040-4039(98)01233-7

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