Asymmetric Synthesis of a New Helix??Forming β??Amino Acid: trans??4??Aminopiperidine??3??carboxylic Acid

M Schinnerl, JK Murray, JM Langenhan…

Index: Schinnerl, Marina; Murray, Justin K.; Langenhan, Joseph M.; Gellman, Samuel H. European Journal of Organic Chemistry, 2003 , # 4 p. 721 - 726

Full Text: HTML

Citation Number: 38

Abstract

Abstract We report a synthesis of a protected derivative of trans-4-aminopiperidine-3- carboxylic acid (APiC). The route provides either enantiomer. All intermediates are purified by crystallization, and large-scale preparation is therefore possible. An analogous route provides either enantiomer of trans-2-aminocyclohexanecarboxylic acid (ACHC). We have previously shown that β-peptide oligomers containing ACHC adopt a helical conformation ...

Related Articles:

Design and syntheses of melanocortin subtype-4 receptor agonists. Part 2: Discovery of the dihydropyridazinone motif

[Bioorganic and Medicinal Chemistry Letters, , vol. 15, # 18 p. 4023 - 4028]

PIPERIDINE DERIVATIVES. XI. 3-CARBETHOXY-4-PIPERIDONE AND 4-PIPERIDONE HYDROCHLORIDE

[Journal of the American Chemical Society, , vol. 53, p. 2692,2696]

PIPERIDINE DERIVATIVES. XI. 3-CARBETHOXY-4-PIPERIDONE AND 4-PIPERIDONE HYDROCHLORIDE

[Journal of the American Chemical Society, , vol. 53, p. 2692,2696]

More Articles...