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Diastereoselective Addition of n-Butyllithium to 2-Phenylpropanal: A Reassessment of the Solvent and Temperature Effects

✍ Scribed by Prof. Dr. Gianfranco Cainelli; Dr. Daria Giacomini; P. Galletti; A. Marini


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
452 KB
Volume
35
Category
Article
ISSN
0044-8249

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📜 SIMILAR VOLUMES


Temperature and Solvent Effect on the Nu
✍ Prof. Dr. Gianfranco Cainelli; Dr. Daria Giacomini; Dr. Martin Walzl 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 342 KB 👁 1 views

Are the Felkin–Ahn and Cram chelate models reliable? These models predict asymmetric induction without consideration of solvent and temperature. However, the addition of __n__‐butyllithium to the __N__‐(trimethylsily)imine of (2__S__)‐lactal leads to __syn/anti__ ratios between 98:2 and 28:72 when p

Diastereoselective Conjugate Addition Re
✍ Artur M. S. Silva; Lúcia M. P. M. Almeida; Hilário R. Tavares; José A. S. Cavale 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 233 KB 👁 2 views

2-hydroxyphenyl)-2,4dimethyl-1,5-pentanediones / NMR spectroscopy The diastereoselective synthesis of 3-aryl-1,5-bis(2-hydroxypropiophenone with appropriate benzaldehyde derivatives. The structures and stereochemistry of the hydroxyphenyl)-2,4-dimethyl-1,5-pentanediones has been carried out by conj