Stereoselective Lewis base catalyzed formal 1,3-dipolar cycloaddition of azomethine imines with mixed anhydrides-Reference-Cited by-同舟云学术

Stereoselective Lewis base catalyzed formal 1,3-dipolar cycloaddition of azomethine imines with mixed anhydrides

Published:2015 Issue:2 Volume:6 Page:1252-1257
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Hesping Lena¹²³⁴,Biswas Anup¹²³⁴,Daniliuc Constantin G.¹²³⁴,Mück-Lichtenfeld Christian¹²³⁴,Studer Armido¹²³⁴

Affiliation:

1. Organisch-Chemisches Institut

2. Westfälische Wilhelms-Universität Münster Corrensstrasse 40

3. 48149 Münster

4. Germany

Abstract

Pyrazolidinones with a tetrahydroisoquinoline core are obtained with excellent diastereocontrol and high enantioselectivity. Theoretical studies give insight on the reaction mechanism.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/SC/C4SC02612H

Reference63 articles.

1. Ecteinascidin 743: a novel anticancer drug with a unique mechanism of action

2. Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics

3. Enantioselective Synthesis of (+)-(S)-Laudanosine and (-)-(S)-Xylopinine

4. β-Phenylethylamines and the isoquinoline alkaloids

5. Synthesis of (–)-(S)-Norlaudanosine, (+)-(R)-O,O-Dimethylcoclaurine, and (+)-(R)-Salsolidine by Alkylation of an α-Aminonitrile

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