(R)-alpha-Aminoadipic acid: an interesting chiral pool building block

Sadiq A, Sewald N (2012)
ARKIVOC 2012(5): 28-36.

Journal Article | Published | English

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Abstract
(R)-alpha-Aminoadipic acid is available on a large scale by enzymatic cleavage from cephalosporin C (CephC) in the production of 7-aminocephalosporanic acid (7-ACA). It can be converted into other interesting enantiomerically pure compounds, e. g. derivatives of (R)-pipecolic acid (R-piperidine-2-carboxylic acid), (R)-6-oxopiperidine-2-carboxylic acid, (R)-1,2,3,4-tetrahydropyridine-2(2H)-carboxylates, and other compounds obtained by further conversions of these products.
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Sadiq A, Sewald N. (R)-alpha-Aminoadipic acid: an interesting chiral pool building block. ARKIVOC. 2012;2012(5):28-36.
Sadiq, A., & Sewald, N. (2012). (R)-alpha-Aminoadipic acid: an interesting chiral pool building block. ARKIVOC, 2012(5), 28-36.
Sadiq, A., and Sewald, N. (2012). (R)-alpha-Aminoadipic acid: an interesting chiral pool building block. ARKIVOC 2012, 28-36.
Sadiq, A., & Sewald, N., 2012. (R)-alpha-Aminoadipic acid: an interesting chiral pool building block. ARKIVOC, 2012(5), p 28-36.
A. Sadiq and N. Sewald, “(R)-alpha-Aminoadipic acid: an interesting chiral pool building block”, ARKIVOC, vol. 2012, 2012, pp. 28-36.
Sadiq, A., Sewald, N.: (R)-alpha-Aminoadipic acid: an interesting chiral pool building block. ARKIVOC. 2012, 28-36 (2012).
Sadiq, Amina, and Sewald, Norbert. “(R)-alpha-Aminoadipic acid: an interesting chiral pool building block”. ARKIVOC 2012.5 (2012): 28-36.
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