4.4 Article

Total synthesis of atorvastatin via a late-stage, regioselective 1,3-dipolar munchnone cycloaddition

期刊

TETRAHEDRON LETTERS
卷 56, 期 23, 页码 3208-3211

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2014.12.104

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Munchnone; 1,3-Dipolar cycloaddition; Atorvastatin; Pyrrole; Mesoionic

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Atorvastatin was prepared in seven steps from commercially available 4-fluorophenylacetic acid. The key 1,3-dipolar cycloaddition was conducted regioselectively using a complex munchnone which was prepared in five steps on decagram scale. (C) 2015 Elsevier Ltd. All rights reserved.

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