Theoretical and Experimental Studies of Asymmetric Organozinc Additions to Benzaldehyde Catalyzed by Flexible and Constrained γ-Amino Alcohols

Manoranjan Panda; Puay-Wah Phuan; Marisa C. Kozlowski

doi:10.1021/jo0262210

journal article Dec 24, 2002

Theoretical and Experimental Studies of Asymmetric Organozinc Additions to Benzaldehyde Catalyzed by Flexible and Constrained γ-Amino Alcohols

Manoranjan Panda Puay-Wah Phuan Marisa C. Kozlowski

The Journal of Organic Chemistry Vol. 68 No. 2 pp. 564-571 · American Chemical Society (ACS)

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We independently located the 6/6 transition structures for the ligands1−3,similar to those reported by Norrby et al. in ref 18, while locating the different possible 6/4/4 transition structures at the PM3 level (see Supporting Information). The PM3 calculations were done using SPARTAN version 5.0. Wavefunction, Inc., 18401 Von Karman Avenue, Suite 370, Irvine, CA 92612.

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Details

Published: Dec 24, 2002
Vol/Issue: 68(2)
Pages: 564-571

Authors

M

Manoranjan Panda

Department of Chemistry, Roy and Diana Vagelos Laboratories, University of Pennsylvania, Philadelphia, Pennsylvania 19104

P

Puay-Wah Phuan

Department of Chemistry, Roy and Diana Vagelos Laboratories, University of Pennsylvania, Philadelphia, Pennsylvania 19104

M

Marisa C. Kozlowski

Department of Chemistry, Roy and Diana Vagelos Laboratories, University of Pennsylvania, Philadelphia, Pennsylvania 19104

Cite This Article

Manoranjan Panda, Puay-Wah Phuan, Marisa C. Kozlowski (2002). Theoretical and Experimental Studies of Asymmetric Organozinc Additions to Benzaldehyde Catalyzed by Flexible and Constrained γ-Amino Alcohols. The Journal of Organic Chemistry, 68(2), 564-571. https://doi.org/10.1021/jo0262210

Theoretical and Experimental Studies of Asymmetric Organozinc Additions to Benzaldehyde Catalyzed by Flexible and Constrained γ-Amino Alcohols

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