Double asymmetric induction in intramolecular C-H insertion reactions of α-diazo β-keto esters

Article abstract of DOI:10.1080/00397919408010251

A new double asymmetric induction in C-C bond formation has been achieved by the use of dirhodium(II) tetrakis[N-phthaloyl-(R) or (S)-phenyl-alaninate] as a homochiral catalyst in intramolecular C-H insertion of α-diazo β-keto esters of homochiral alcohol

Full text of DOI:10.1080/00397919408010251

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Synthetic Communications: An
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Double Asymmetric Induction
in Intramolecular C-H Insertion
Reactions of α-Diazo β-Keto
Esters
Shun-ichi Hashimoto a , Nobuhide Watanabe a ,
Katsuhiro Kawano a & Shiro Ikegami a
a Faculty of Pharmaceutical Sciences, Teikyo
University Sagamiko, Kanagawa, 199-01, Japan
Published online: 23 Sep 2006.
To cite this article: Shun-ichi Hashimoto , Nobuhide Watanabe , Katsuhiro Kawano &
Shiro Ikegami (1994): Double Asymmetric Induction in Intramolecular C-H Insertion
Reactions of α-Diazo β-Keto Esters, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 24:22, 3277-3287
To link to this article: http://dx.doi.org/10.1080/00397919408010251
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