TRICARBONYLCHROMIUM(0) PROMOTED STEREOSELECTIVE CYCLIZATIONS OF THE N-3,4-DIMETHOXYPHENETHYL DERIVATIVES OF THE 1-PHENYL ETHANOLAMINES HALOSTACHINE, EPHEDRINE AND PSEUDOEPHEDRINE TO 1-PHENYL-N-METHYL-7,8-DIMETHOXY-1,2,4,5-TETRAHYDROBENZAZEPINES

Acid promoted cyclisation of homochiral (R)-N-(3,4-dimethoxyphenethyl)-halostachine proceeds with almost total racemisation to yield 1-phenyl-N-methyl-1,2,4,5-tetrahydrobenz[d]azepine (e.e. 6%). Coordination of the cyclisation precursor to the tricarbonylchromium(0) moiety renders the cyclisation co...

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Bibliographic Details
Main Authors: Coote, S, Davies, S, Middlemiss, D, Naylor, A
Format: Journal article
Language:English
Published: 1990