Stereoselective Synthesis of (±)-methyl Nonactate

Published

Journal Article

Racemic methyl nonactate has been prepared in 11 steps from 2,2-dimethyl-3(2H)-furanone with the diastereoisomeric relationships between C-2 and C-3, C-3 and C-6, and C-6 and C-8 established with stereoselectivities of 32:1, 50:1, and 24:1, respectively. © 1987, American Chemical Society. All rights reserved.

Full Text

Published version (via Digital Object Identifier)

Duke Authors

Baldwin, Steven W.

Cited Authors

Baldwin, SW; Mclver, JM

Published Date

January 1, 1987

Published In

The Journal of Organic Chemistry

Volume / Issue

52 / 2

Start / End Page

320 - 322

Electronic International Standard Serial Number (EISSN)

1520-6904

International Standard Serial Number (ISSN)

0022-3263

Digital Object Identifier (DOI)

10.1021/jo00378a043

Citation Source

Scopus