NOVEL APPROACH TO SEVEN-MEMBERED RINGS BY THE INTRAMOLECULAR TANDEM CYCLOPROPANATION/COPE REARRANGEMENT SEQUENCE

DOI: 10.1016/0040-4039(88)85312-7

Source and publish data:

Tetrahedron Letters p. 975 - 978 (1988)

Update date:2022-08-04

Topics:

Authors:

Davies, Huw M. L.

Oldenburg, C. E. Michael

McAfee, Melinda J.

Nordahl, J. Greg

Henretta, John P.

Romines, Karen R.

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Article abstract of DOI:10.1016/0040-4039(88)85312-7

The intramolecular tandem cyclopropanation/Cope rearrangement sequence between rhodium(II) acetate stabilized vivylcarbenoids and dienes is a feasible method for the stereospecific synthesis of fused seven-membered rings.

Full text of DOI:10.1016/0040-4039(88)85312-7

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