A Highly Diastereoselective Recognition Process as the Basis for the Resolution of Palladatricyclo[4.1.0.02,4]heptanes-Reference-Cited by-同舟云学术

A Highly Diastereoselective Recognition Process as the Basis for the Resolution of Palladatricyclo[4.1.0.02,4]heptanes

Published:2012-01-09 Issue:2 Volume:31 Page:523-526
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Hashmi A. Stephen K.¹²,Grundl Marc A.²,Riedel Dominic¹,Rudolph Matthias¹,Bats Jan W.³

Affiliation:

1. Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany

2. Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany

3. Institut für Organische Chemie und Chemische Biologie, Johann Wolfgang Goethe-Universität Frankfurt, Max-von-Laue-Straße 7, 60438 Frankfurt, Germany

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om2009952

Reference18 articles.

1. Different Diastereoselectivities in the Stereoselective Oxidative Cyclization of Two Cyclopropenes at Palladium(0)

2. Tetraallyl (2,2′-bipyridyl)-rac-3,3,7,7-tetramethyl-trans-5-palladatricyclo[4.1.0.02,4]heptane-1,2,4,6-tetracarboxylate above and below the phase-transition temperature of 194 K

3. Die erste und hochdiastereoselektive Synthese von Palladepanen

4. Angew. Chem., Int. Ed. Engl. 1999, 38, 3370–3373.

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