Chirale 3-Aminopropanole, 1. Mitt. Synthese der Racemate und der Enantiomere-Reference-Cited by-同舟云学术

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Chirale 3-Aminopropanole, 1. Mitt. Synthese der Racemate und der Enantiomere

Published:1985 Issue:7 Volume:318 Page:593-600
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:de
Short-container-title:Arch. Pharm. Pharm. Med. Chem.

Author:

Knabe Joachim,Buchheit Wolfgang

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Reference31 articles.

1. Aus der Dissertation Saarbrücken 1982.

2. Über die Reduktion substituierter Cyanessigsäure‐äthylester (Reduktionen mit LiALH 4 VIII. Mitteil.

3. Olin Mathieson Chemical Corp., Erf. US Pat. 2940971 (14. 6. 1960);

4. 2-Amino-5,6-dihydro-1,3-oxazines. The Reduction of Carboxylic Esters with Sodium Borohydride1

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1. An efficient method for the preparation of mono α-aryl derivatives of diethyl malonate and ethyl cyanoacetate using ethyl-1-imidazole carbamate (EImC);Tetrahedron Letters;2012-02

2. Palladium-Catalyzed Arylation of Malonates and Cyanoesters Using Sterically Hindered Trialkyl- and Ferrocenyldialkylphosphine Ligands;The Journal of Organic Chemistry;2001-12-29

3. Palladium-Catalyzed Arylation of Ethyl Cyanoacetate. Fluorescence Resonance Energy Transfer as a Tool for Reaction Discovery;Journal of the American Chemical Society;2001-04-24

4. A Versatile Method for the Synthesis ofcis-2-Aminomethylcyclanols;Synthetic Communications;1998-06

5. Ring-chain tautomerism and three- to four-component equilibria in fused-ring tetrahydro-1,3-oxazines;Tetrahedron;1991-01

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