N-Arylated 3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push-Pull Chromophores-Reference-Cited by-同舟云学术

N-Arylated 3,5-Dihydro-4H-dinaphtho[2,1-c:1′,2′-e]azepines: Axially Chiral Donors with High Helical Twisting Powers for Nonplanar Push-Pull Chromophores

Published:2009-09-14 Issue:36 Volume:15 Page:9005-9016
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Frank Brian B.,Camafort Blanco Berta,Jakob Samuel,Ferroni Fiammetta,Pieraccini Silvia,Ferrarini Alberta,Boudon Corinne,Gisselbrecht Jean-Paul,Seiler Paul,Spada Gian Piero,Diederich François

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.200900913/fullpdf

Reference101 articles.

1. A Scalable Synthesis of (R)-3,5-Dihydro-4H-dinaphth[2,1-c:1‘2‘-e]azepine

2. Effects of Aromatic Substituents on Binaphthyl-Based Chiral Spiro-Type Ammonium Salts in Asymmetric Phase-Transfer Reactions

3. New axially chiral atropos and tropos secondary diamines as ligands for enantioselective intramolecular hydroamination

4. Synthesis of aminophosphines containing a chiral dinaphthoazepine entity and their use in asymmetric catalysis

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