Synthesis of thePreininger-Alkaloid and its Enantioselective Reduction to Macrostomine-Reference-Cited by-同舟云学术

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Synthesis of thePreininger-Alkaloid and its Enantioselective Reduction to Macrostomine

Published:1991 Issue:5 Volume:324 Page:275-281
ISSN:0365-6233
Container-title:Archiv der Pharmazie
language:de
Short-container-title:Arch. Pharm. Pharm. Med. Chem.

Author:

Mahboobi Siavosh,Wiegrebe Wolfgang

Publisher

Wiley

Subject

Drug Discovery,Pharmaceutical Science

Reference25 articles.

1. Isolation and chemistry of the alkaloids from Papaver macrostomum BOISS. et HUET

2. 4-Substituted 6,7-dimethoxyisoquinolines

3. α-Methyl α-Amino Acids. II.1 Derivatives of DL-Phenylalanine

4. Advanced Organic Chemistry, 3rd ed., p. 495, J. Wiley & Sons, New York., 1985.

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1. A Five-Step Synthesis of (S)-Macrostomine from (S)-Nicotine;Organic Letters;2010-09-22

2. ChemInform Abstract: Synthesis of the Preininger Alkaloid (I) and Its Enantioselective Reduction to Macrostomine.;ChemInform;2010-08-22

3. Heterocyclization reactions involving thiols;Russian Journal of Organic Chemistry;2006-05

4. Electron Impact Induced Fragmentation of Aromatic Alkoxyimines II [5]. Formation and Transformation of Heterocyclic Radical Cations in the Gas Phase a;Monatshefte f�r Chemie / Chemical Monthly;2003-02-01

5. Syntheses of (RS)- and (S)-(−)-Nazlinin and (RS)- and (+)-6-Azacyclodeca[5,4-b]indol-1-amine;Archiv der Pharmazie;1995

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