Efficient resolution of (±)-trans-2,3-diphenylpiperazine using (1S)-(+)10-camphorsulfonic acid and enrichment of enantiomeric purity of non-racemic 2,3-diphenylpiperazine using different achiral acids

7Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Enantiomerically pure (R,R)-(+)-2,3-diphenylpiperazine with 98% ee was obtained by resolution of the corresponding racemic mixture using (15)-(+)-10-camphorsulfonic acid. The partially resolved enriched sample of (S,S)-(-)-2,3-diphenylpiperazine with 73% ee was purified to obtain samples of 97% ee using different achiral acids via the preparation of either homochiral or heterochiral hydrogen bonded aggregates. © Indian Academy of Sciences.

Cite

CITATION STYLE

APA

Vairaprakash, P., & Periasamy, M. (2008). Efficient resolution of (±)-trans-2,3-diphenylpiperazine using (1S)-(+)10-camphorsulfonic acid and enrichment of enantiomeric purity of non-racemic 2,3-diphenylpiperazine using different achiral acids. Journal of Chemical Sciences, 120(1), 175–179. https://doi.org/10.1007/s12039-008-0020-5

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free