Enantiomerically Pure N Chirally Substituted 1,3-Benzazaphospholes: Synthesis, Reactivity toward tBuLi, and Conversion to Functionalized Benzazaphospholes and Catalytically Useful Dihydrobenzazaphospholes-Reference-Cited by-同舟云学术

Enantiomerically Pure N Chirally Substituted 1,3-Benzazaphospholes: Synthesis, Reactivity toward tBuLi, and Conversion to Functionalized Benzazaphospholes and Catalytically Useful Dihydrobenzazaphospholes

Published:2014-01-23 Issue:3 Volume:33 Page:804-816
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Ghalib Mohammed¹,Jones Peter G.²,Lysenko Sergej²,Heinicke Joachim W.¹

Affiliation:

1. Institut für Chemie und Biochemie, Ernst-Moritz-Arndt-Universität Greifswald, 17487 Greifswald, Germany

2. Institut für Anorganische und Analytische Chemie der Technischen Universität Braunschweig, 38023 Braunschweig, Germany

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om401184n

Reference57 articles.

1. Anellated Heterophospholes and Phospholides and Analogies with Related Non-Phosphorus Systems

2. cSchmidpeter, A.InPhosphorus-Carbon Heterocyclic Chemistry: The Rise of a New Domain;Mathey, F., Ed.Pergamon:Amsterdam, 2001; p363.

3. π-Excess σ2P ligands: synthesis of biaryl-type 1,3-benzazaphosphole hybrid ligands and formation of P^P′–M(CO)4 chelate complexes

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