Reduction of 2-alkyl-2-carbomethoxy-cyclopentanone derivatives with sodium borohydride. Part 2. The elucidation of the diastereoselective control

Article abstract of DOI:10.1080/00397919708004185

The synthesis and reduction of four new 2-substituted β-keto-ester derivatives (6-9) employing inexpensive sodium borohydride, were achieved to evaluate the diastereoselectivity of the reduction process of 2-allyl-2- carbomethoxy cyclopentanone derivative

Full text of DOI:10.1080/00397919708004185

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Synthetic Communications: An
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Organic Chemistry
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Reduction of 2-Alkyl-2-
carbomethoxy-cyclopentanone
Derivatives with Sodium
Borohydride. II. The
Elucidation of the
Diastereoselective Control
Lis H. P. Teixeira a , Eliezer J. Barreiro a & Carlos A.
M. Fraga a
a Laboratório de Avaliação e Sintese de
Subst[acaron]ncias Bioativas (LASSBio) , Faculdade
de Farmácia, Universidade Federal do Rio de
Janeiro , C.P. 68006, ZIP-21944-910, Rio de Janeiro,
R.J., Brazil E-mail:
Published online: 22 Aug 2006.
To cite this article: Lis H. P. Teixeira , Eliezer J. Barreiro & Carlos A. M. Fraga
(1997) Reduction of 2-Alkyl-2-carbomethoxy-cyclopentanone Derivatives with
Sodium Borohydride. II. The Elucidation of the Diastereoselective Control , Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 27:18, 3241-3257, DOI: 10.1080/00397919708004185
To link to this article: http://dx.doi.org/10.1080/00397919708004185
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