Studies in macrolide synthesis: A novel cyclodimerisation approach to the synthesis of elaiophylin using a double stille cross-coupling reaction

DOI: 10.1016/S0040-4039(96)02395-7

Source and publish data:

Tetrahedron Letters p. 695 - 698 (1997)

Update date:2022-08-05

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Authors:

Paterson, Ian

Man, Jocelyn

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Article abstract of DOI:10.1016/S0040-4039(96)02395-7

The 16-membered macrodiolide 4, corresponding to the macrocyclic core of elaiophylin (1), was prepared via the copper-mediated cyclodimerisation of stannane 3.

Full text of DOI:10.1016/S0040-4039(96)02395-7

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