Asymmetric synthesis XXVI: Catalytic enantioselective syntheses of β-hydroxy esters via double chiral induction in asymmetric Reformatsky reactions

Article abstract of DOI:10.1080/00397919708006081

Catalytic asymmetric Reformatsky reactions of benzaldehyde with optically active menthyl bromoacetates in the presence of Zn-Cu couple were performed using 0.25 equiv. of (1R,2S) or (1S,2R)-N,N-dimethyl-2-amino-1,2-diphenyl ethanol as chiral ligand to obt

Full text of DOI:10.1080/00397919708006081

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Asymmetric Syntheses XXVI:
Catalytic Enantioselective
Syntheses of β-Hydroxy Esters
via Double Chiral Induction
in Asymmetric Reformatsky
Reactions
a
a
a
Aiqiao Mi , Zhaoyang Wang , Junmei Zhang &
a
Yaozhong Jiang
a
Union Laboratory of Asymmetric Synthesis,
Chengdu Institute of Organic Chemistry, Chinese
Academy of Sciences, Chengdu, 610041, China
Version of record first published: 22 Aug 2006.
To cite this article: Aiqiao Mi , Zhaoyang Wang , Junmei Zhang & Yaozhong Jiang
(1997): Asymmetric Syntheses XXVI: Catalytic Enantioselective Syntheses of β-Hydroxy
Esters via Double Chiral Induction in Asymmetric Reformatsky Reactions, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 27:9, 1469-1473
To link to this article: http://dx.doi.org/10.1080/00397919708006081
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