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Studies of Diastereoselectivity in Conjugate Addition of Organoaluminum Reagents to ( R )-[( p -Tolylsulfinyl)methyl]quinols and Derivatives

✍ Scribed by Carreño, M. Carmen; Pérez González, Manuel; Ribagorda, María; Houk, K. N.


Book ID
126914157
Publisher
American Chemical Society
Year
1998
Tongue
English
Weight
185 KB
Volume
63
Category
Article
ISSN
0022-3263

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ChemInform Abstract: Diastereoselective
✍ M. C. CARRENO; M. PEREZ GONZALEZ; M. RIBAGORDA; J. FISCHER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Diastereoselective Uncatalyzed Conjugate Addition of Organoaluminum Reagents: Efficient Desymmetrization of (R)-((p-Tolylsulfinyl)methyl) quinols. -The exclusive 1,4-addition of organoaluminum reagents to (I) and (IV) proceeds without metal catalysts under mild conditions with good yields. The gen