INTRAMOLECULAR CYCLISATION-N-DEALKYLATION OF AZETIDINE-3-ACETIC ACIDS

DOI: 10.1016/S0040-4039(00)92311-6

Source and publish data:

Tetrahedron Letters p. 4799 - 4800 (1991)

Update date:2022-07-31

Topics:

Authors:

Bartholomew, David

Stocks, Michael J.

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Article abstract of DOI:10.1016/S0040-4039(00)92311-6

N-Aryl-azetidine-3-acetic acids are converted to pyrrolidinones when treated with oxalyl chloride.The intramolecular cyclisation-N-dealkylation reaction occurs via an azabicyclic intermediate.N-Aryl-azetidine-3-acetic acids are prepared from N-aryl-3-(chl

Full text of DOI:10.1016/S0040-4039(00)92311-6

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