ChemInform Abstract: Unusual N-Acylation of Sterically Congested trans-4,5-Disubstituted 2-Imidazolidinones: Remarkably Facile C—C Bond Formation.

ChemInform Abstract: Enantiospecific For

ChemInform Abstract: Enantiospecific Formation of trans-1,3-Disubstituted Tetrahydro-β- carbolines by the Pictet-Spengler Reaction and Conversion of cis Diastereomers into Their trans Counterparts by Scission of the C-1/N-2 Bond.

✍ E. D. COX; L. K. HAMAKER; J. LI; P. YU; K. M. CZERWINSKI; L. DENG; D. W. BENNETT 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

Enantiospecific Formation of trans-1,3-Disubstituted Tetrahydro-βcarbolines by the Pictet-Spengler Reaction and Conversion of cis Diastereomers into Their trans Counterparts by Scission of the C-1/N-2 Bond. -The factors which effect the stereoselective formation of trans-products in the Pictet-Spen