The Ullmann Coupling Reaction of Axially Chiral (S)-2,2′-Bis(1-iodo-2-naphthyloxycarbonyl)-1,1′-binaphthyl
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/58/4/58_4_1345/_pdf
Reference6 articles.
1. Tetrahedron report number 163
2. The Asymmetric Ullmann Coupling Reaction of Chiral Diol Diesters of 1-Bromo-2-naphthoic Acid and 2-Halo-3-nitrobenzoic Acids: Highly Diastereoselective Synthesis of Atropisomeric 6,6′-Dinitrodiphenic Acids
3. Synthetic studies on lignan lactones: aryl dithiane route to (.+-.)-podorhizol and (.+-.)-isopodophyllotoxone and approaches to the stegane skeleton
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1. A new route to 2,2′,3,3′-tetrasubstituted binaphthyls;Tetrahedron Letters;2009-05
2. Iodine-Promoted Efficient Homocoupling of Arylboronic Acids in PEG-400 under Aerobic Conditions;European Journal of Organic Chemistry;2009-05
3. Dimeric Orsellinic Acid Derivatives: Valuable Intermediates for Natural Product Synthesis;European Journal of Organic Chemistry;2007-04
4. Practical synthetic protocols of enantiopure 1,1′-binaphthyl-2,2′-dicarboxylic acid and 2,2′-dicyano-1,1′-binaphthyl starting from optically active dibromide precursor;Tetrahedron Letters;2004-04
5. Cu, Ni, and Pd Mediated Homocoupling Reactions in Biaryl Syntheses: The Ullmann Reaction;Organic Reactions;2004-01-28
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