A convenient route to spiropyrrolidinyl-oxindole alkaloids via C-3 substituted ene-pyrrolidine carbamate radical cyclization

DOI: 10.1016/S0040-4039(98)00193-2

Source and publish data:

Tetrahedron Letters p. 2331 - 2332 (1998)

Update date:2022-08-05

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Authors:

Cossy, Janine

Cases, Manuel

Gomez Pardo, Domingo

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Article abstract of DOI:10.1016/S0040-4039(98)00193-2

A short access to spiropyrrolidinyl-oxindole alkaloids via a substituted ene-pyrrolidine carbamate, synthesized from the commercially available tert- butyl 1-pyrrolidine carboxylate, is described.

Full text of DOI:10.1016/S0040-4039(98)00193-2

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