The Journal of Organic Chemistry

Enzymic hydrolysis of ethyl 3-hydroxy-3-phenylpropanoate: observations on an enzyme active-site model

NW Boaz

Index: Boaz, Neil W. Journal of Organic Chemistry, 1992 , vol. 57, # 15 p. 4289 - 4292

Full Text: HTML

Citation Number: 67

Abstract

Alders and even organocopper conjugate additiong reactions, attesting to the attractiveness of this class of compounds. These latter reactions all have drawbacks, most notably the widespread need for stoichiometric chiral reagents. Clearly, the most efficient synthetic

Related Articles:

Stereoselective synthesis of (S)-dapoxetine: a chiral auxiliary mediated approach

[Khatik, Gopal L.; Sharma, Ratnesh; Kumar, Varun; Chouhan, Mangilal; Nair, Vipin A. Tetrahedron Letters, 2013 , vol. 54, # 45 p. 5991 - 5993]

A New Approach for the Chemoselective Debromination of Chiral Bromohydrins. Toward the Development of a Very General Approach to Enantiopure α- …

[Wang, Ying-Chuan; Yan, Tu-Hsin Journal of Organic Chemistry, 2000 , vol. 65, # 20 p. 6752 - 6755]

(1S, 2S)-1-Amino-2-hydroxy-1, 2, 3, 4-tetrahydronaphthalene: a new chiral auxiliary for asymmetric Reformatsky reactions

[Orsini, Fulvia; Sello, Guido; Manzo, Angelo Maria; Lucci, Elvira Maria Tetrahedron Asymmetry, 2005 , vol. 16, # 11 p. 1913 - 1918]

Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates

[Evans, D. A.; Bartroli, J.; Shih, T. L. Journal of the American Chemical Society, 1981 , vol. 103, # 8 p. 2127 - 2129]

Asymmetric Aldol Type Reactions of Acetate Imide Enolates

[Yan, Tu-Hsin; Hung, An-Wei; Lee, Hui-Chun; Chang, Chii-Shin; Liu, Wen-Hung Journal of Organic Chemistry, 1995 , vol. 60, # 11 p. 3301 - 3306]

More Articles...