TRANSAMIDATION REACTIONS IN THE FORMATION OF MACROCYCLIC LACTAMS. A TOTAL SYNTHESIS OF CELLACINNINE.

DOI: 10.1016/S0040-4039(00)78723-5

Source and publish data:

Tetrahedron Letters p. 3493 - 3496 (1980)

Update date:2022-08-04

Topics:

Authors:

Wasserman, Harry H.

Robinson, Ralph P.

Matsuyama, Haruo

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Article abstract of DOI:10.1016/S0040-4039(00)78723-5

The macrocyclic spermidine alkaloid, cellacinnine, has been synthetized by methods involving successive ring expansion reactions.One route starts with 4-phenyl-2-azetidinone; another, with piperidazine.

Full text of DOI:10.1016/S0040-4039(00)78723-5

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Product name:1-(4,5-Dihydro-3H-pyrrol-2-yl)-4-phenyl-azetidin-2-one

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