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An amidyl radical cyclisation approach towards the synthesis of beta-lactams
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UNSPECIFIED (1998) An amidyl radical cyclisation approach towards the synthesis of beta-lactams. TETRAHEDRON LETTERS, 39 (10). pp. 1265-1268. ISSN 0040-4039.
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Abstract
Amidyl radicals generated from tributylstannane mediated homolysis of O-benzoyl hydroxamic acid derivatives (2a-d) undergo 4-exo trig cyclisation to furnish beta-lactam derivatives (4a-d). (C) 1998 Elsevier Science Ltd. All rights reserved.
Item Type: | Journal Article | ||||
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Subjects: | Q Science > QD Chemistry | ||||
Journal or Publication Title: | TETRAHEDRON LETTERS | ||||
Publisher: | PERGAMON-ELSEVIER SCIENCE LTD | ||||
ISSN: | 0040-4039 | ||||
Official Date: | 5 March 1998 | ||||
Dates: |
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Volume: | 39 | ||||
Number: | 10 | ||||
Number of Pages: | 4 | ||||
Page Range: | pp. 1265-1268 | ||||
Publication Status: | Published |
Data sourced from Thomson Reuters' Web of Knowledge
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