Synthetic routes towards enantiomerically pure beta-amino acids

Sewald N (2003)
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 42(47): 5794-5795.

Download
Es wurde kein Volltext hochgeladen. Nur Publikationsnachweis!
Zeitschriftenaufsatz | Veröffentlicht | Englisch
Erscheinungsjahr
Zeitschriftentitel
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Band
42
Zeitschriftennummer
47
Seite
5794-5795
ISSN
eISSN
PUB-ID

Zitieren

Sewald N. Synthetic routes towards enantiomerically pure beta-amino acids. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION. 2003;42(47):5794-5795.
Sewald, N. (2003). Synthetic routes towards enantiomerically pure beta-amino acids. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 42(47), 5794-5795. doi:10.1002/anie.200301692
Sewald, N. (2003). Synthetic routes towards enantiomerically pure beta-amino acids. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 42, 5794-5795.
Sewald, N., 2003. Synthetic routes towards enantiomerically pure beta-amino acids. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 42(47), p 5794-5795.
N. Sewald, “Synthetic routes towards enantiomerically pure beta-amino acids”, ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, vol. 42, 2003, pp. 5794-5795.
Sewald, N.: Synthetic routes towards enantiomerically pure beta-amino acids. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION. 42, 5794-5795 (2003).
Sewald, Norbert. “Synthetic routes towards enantiomerically pure beta-amino acids”. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 42.47 (2003): 5794-5795.

9 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Cu-Catalyzed selective cascade sp(3) C-H bond oxidative functionalization towards isoxazoline derivatives.
Wang GW, Cheng MX, Ma RS, Yang SD., Chem Commun (Camb) 51(29), 2015
PMID: 25760469
Manganese(III)-mediated alkenyl C(sp2)-P bond formation from the reaction of β-nitrostyrenes with dialkyl phosphites.
Xue JF, Zhou SF, Liu YY, Pan X, Zou JP, Asekun OT., Org Biomol Chem 13(17), 2015
PMID: 25812140
Syntheses and anti-tubercular activity of β-substituted and α,β-disubstituted peptidyl β-aminoboronates and boronic acids.
Gorovoy AS, Gozhina O, Svendsen JS, Tetz GV, Domorad A, Tetz VV, Lejon T., J Pept Sci 19(10), 2013
PMID: 24014472
Expedient synthesis of a 72-membered isoxazolino-β-ketoamide library by a 2·3-component reaction.
Knapp JM, Zhu JS, Wood AB, Kurth MJ., ACS Comb Sci 14(2), 2012
PMID: 22181856
Microwave-assisted organocatalytic enantioselective intramolecular aza-Michael reaction with α,β-unsaturated ketones.
Fustero S, del Pozo C, Mulet C, Lazaro R, Sánchez-Roselló M., Chemistry 17(50), 2011
PMID: 22083999
Enantioselective Michael addition of alpha-substituted cyanoacetates to vinyl ketones catalyzed by bifunctional organocatalysts.
Liu TY, Li R, Chai Q, Long J, Li BJ, Wu Y, Ding LS, Chen YC., Chemistry 13(1), 2007
PMID: 17039561

Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®

Quellen

PMID: 14673908
PubMed | Europe PMC

Suchen in

Google Scholar