Improved synthesis of both enantiomers of trans-cyclohex-4-ene-1,2-dicarboxylic acid

Citation
A. Bernardi et al., Improved synthesis of both enantiomers of trans-cyclohex-4-ene-1,2-dicarboxylic acid, TETRAHEDR-A, 10(17), 1999, pp. 3403-3407
Citations number
16
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
10
Issue
17
Year of publication
1999
Pages
3403 - 3407
Database
ISI
SICI code
0957-4166(19990827)10:17<3403:ISOBEO>2.0.ZU;2-K
Abstract
A facile synthesis of both enantiomers of trans-cyclohex-4-ene-1,2-dicarbox ylic acid on a multigram scale, that starts from inexpensive, commercially available compounds, is described. (C) 1999 Elsevier Science Ltd. All right s reserved.