Issue 7, 2010

A stereoselective intramolecular cyclopropanation via a de novo class of push–pull carbenes derived from DMDO-epoxidations of chiral ynamides

Abstract

This work describes the first examples of diastereoselective intramolecular cyclopropanations of a de novo class of push–pull carbenes derived from DMDO-epoxidations of chiral ynamides. This reaction sequence essentially constitutes a tandem epoxidation–cyclopropanation that effectively gives rise to a series of structurally unique amido-cyclopropanes. A plausible mechanistic model is proposed revealing insights into this novel cyclopropanation process.

Graphical abstract: A stereoselective intramolecular cyclopropanation via a de novo class of push–pull carbenes derived from DMDO-epoxidations of chiral ynamides

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2010
Accepted
18 Mar 2010
First published
26 Apr 2010

New J. Chem., 2010,34, 1309-1316

A stereoselective intramolecular cyclopropanation via a de novo class of push–pull carbenes derived from DMDO-epoxidations of chiral ynamides

H. Li, J. E. Antoline, J. Yang, Z. F. Al-Rashid and R. P. Hsung, New J. Chem., 2010, 34, 1309 DOI: 10.1039/C0NJ00063A

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