Diastereoselective reaction of aldehydes with 3-bromocyclohexene and tin

Article abstract of DOI:10.1080/00397919408010579

The reaction of 3-bromocyclohexane and powdered tin with aromatic aldehydes and an alkynal provides excellent erythro-selective products, while the corresponding reactions with aliphatic aldehydes proceed with moderate erythroselectivity.

Full text of DOI:10.1080/00397919408010579

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Diastereoselective Reaction
of Aldehydes with 3-
Bromocyclohexene and Tin
Jing-Yao Zhou a , Zhao-Gen Chen a & Shi-Hui Wu a
a Department of Chemistry , Fudan University ,
Shanghai, 200433, CHINA
Published online: 23 Sep 2006.
To cite this article: Jing-Yao Zhou , Zhao-Gen Chen & Shi-Hui Wu (1994)
Diastereoselective Reaction of Aldehydes with 3-Bromocyclohexene and Tin, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 24:18, 2661-2664, DOI: 10.1080/00397919408010579
To link to this article: http://dx.doi.org/10.1080/00397919408010579
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