Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5288814 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
An inherently chiral calix[6]arene possessing a C2-symmetric A-B-H substitution pattern was synthesized via a two step process starting from the parent hexa-t-butylcalix[6]arene. The racemic, inherently chiral compound exists as a single isomer with the 1,4-alternate conformation. The inherent chirality was confirmed by treatment of the racemic compound with Pirkle's reagent to form diastereomeric complexes in solution.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Michael T. Blanda, Lauren Edwards, Ralph Salazar, Mikki Boswell,