Issue 1, 1999

Asymmetric synthesis of (2R,3S )-2,3-epoxyamides via camphor-derived sulfonium ylides

Abstract

Enantiomerically enriched trans-2,3-epoxyamides 3 were prepared by the reaction of aldehydes 2 with camphor-derived chiral sulfonium ylide 1 in good yields and moderate to good ee values. The absolute configuration of the reaction product is also determined by chemical transformations.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1999, 77-80

Asymmetric synthesis of (2R,3S )-2,3-epoxyamides via camphor-derived sulfonium ylides

Y. Zhou, X. Hou, L. Dai, L. Xia and M. Tang, J. Chem. Soc., Perkin Trans. 1, 1999, 77 DOI: 10.1039/A806189K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements