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Aryloxy tetrazoles with axial chirality: Synthesis and partial resolution of 5‐(1‐(2‐methoxynaphthalen‐1‐yl)naphthalen‐2‐yloxy)‐1 H ‐tetrazole

Aryloxy tetrazoles with axial chirality: Synthesis and partial resolution of... 5‐(1‐(2‐Methoxynaphthalen‐1‐yl)naph‐ thalen‐2‐yloxy)‐1H‐tetrazole as the first aryloxy tetrazole with axial chirality was synthesized. Partial resolution was achieved using (S)‐proline and methylbenzylamine as the resolving agents. Best results were obtained using methylbenzylamine with 75–85% ee. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:416–419, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20241 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Heteroatom Chemistry Wiley

Aryloxy tetrazoles with axial chirality: Synthesis and partial resolution of 5‐(1‐(2‐methoxynaphthalen‐1‐yl)naphthalen‐2‐yloxy)‐1 H ‐tetrazole

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References (24)

Publisher
Wiley
Copyright
Copyright © 2006 Wiley Periodicals, Inc.
ISSN
1042-7163
eISSN
1098-1071
DOI
10.1002/hc.20241
Publisher site
See Article on Publisher Site

Abstract

5‐(1‐(2‐Methoxynaphthalen‐1‐yl)naph‐ thalen‐2‐yloxy)‐1H‐tetrazole as the first aryloxy tetrazole with axial chirality was synthesized. Partial resolution was achieved using (S)‐proline and methylbenzylamine as the resolving agents. Best results were obtained using methylbenzylamine with 75–85% ee. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:416–419, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20241

Journal

Heteroatom ChemistryWiley

Published: Jan 1, 2006

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