A convenient resolution of pipecolic acid using a metal complex as the chiral auxiliary-Reference-Cited by-同舟云学术

A convenient resolution of pipecolic acid using a metal complex as the chiral auxiliary

Published:2007-07-16 Issue:16 Volume:60 Page:1789-1794
ISSN:0095-8972
Container-title:Journal of Coordination Chemistry
language:en
Short-container-title:Journal of Coordination Chemistry

Author:

Clement Julia L.¹,Leverett Peter²,Vagg Robert S.³,Williams Peter A.²

Affiliation:

1. a Chemistry Department , Cardiff University , P.O. Box 912, Cardiff CF1 3TB, Wales, United Kingdom

2. b School of Natural Sciences, University of Western Sydney , Locked Bag 1797, Penrith South, DC NSW 1797, Australia

3. c School of Chemistry, Macquarie University , NSW 2109, Australia

Publisher

Informa UK Limited

Subject

Materials Chemistry,Physical and Theoretical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/08912960701189883

Reference9 articles.

1. M , Newman . 1981. Optical resolution procedures for chemical compounds, Vol. 2, 216Riverdale, New York: Optical Resolution Information Center, Manhattan College.

2. CHIRAL METAL COMPLEXES. PART 52. THE STRUCTURES OF CO-CRYSTALLISED DIASTEREOISOMERIC DNA PROBES SHOWING INTRAMOLECULAR π-π INTERACTIONS

3. Chiral metal complexes Part 39. Resolution of α-methyltryptophane via coordination to an optically active metal complex

4. Chiral metal complexes. 32. Use of an optically active complex for a nearly absolute chiral induction

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2. Crystal structures of resorcin[4]arene and pyrogallol[4]arene complexes with DL-pipecolinic acid. Model compounds for the recognition of the pipecolinyl ring, a key fragment of FK506, through C–H⋯π interaction;Journal of Molecular Structure;2014-01