Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/28935
Title: Stereospecific synthesis of 2-phthalimido-2a,3,4,5-tetrahydro-1H-azeto[2,1-d][1,5] benzothiazepin-1-ones
Authors: Xu, J
Zuo, G
Zhang, Q
Chan, WL
Issue Date: 2002
Source: Heteroatom chemistry, 2002, v. 13, no. 3, p. 276-279 How to cite?
Journal: Heteroatom Chemistry 
Abstract: Stereospecific synthesis of 2a,4-disubstituted 2-phthalimido-2a,3,4,5-terahydro-1H-azeto[2,1-d][1,5]benzothiazepin-1-ones was discussed. The stereochemistry for the cycloaddition reaction was also presented. 2a, 4-disubstituted 2-phthalimido-2a,3,4,5-tetrahydro-1H-azeto[2,1-d][1,5]benzothiazepin-1-ones were synthesized by cycloaddition reactions of 2,4-disubstituted 2,3-dihydro-1,5-benzothiazepines and phthalimidoketene, generated from phthalimidoacetyl chloride, in the presence of triethylamine in anhydrous benzene.
URI: http://hdl.handle.net/10397/28935
ISSN: 1042-7163
DOI: 10.1002/hc.10029
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