Synthesis of dolastatin G and nordolastatin G, cytotoxic 35-membered cyclodepsipeptides of marine origin

DOI: 10.1016/0040-4039(96)01653-X

Source and publish data:

Tetrahedron Letters p. 7299 - 7302 (1996)

Update date:2022-08-03

Topics:

Authors:

Mutou, Tsuyoshi

Kondo, Takashi

Shibata, Takunobu

Ojika, Makoto

Kigoshi, Hideo

Yamada, Kiyoyuki

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Article abstract of DOI:10.1016/0040-4039(96)01653-X

The synthesis of dolastatin G (1) and nordolastatin G (2), new cytotoxic cyclodepsipeptides from the Japanese sea hare Dolabella auricularia, was achieved enantioselectively, and the present result confirmed their stereostructures unambiguously.

Full text of DOI:10.1016/0040-4039(96)01653-X

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