Sequential Elimination−Cyclopropanation Reactions Promoted by Samarium: Highly Diastereoselective Synthesis of Cyclopropylamides
摘要:
trans-Cyclopropanamides were obtained, in high yield, from 2-chloro-3-hydroxyamides by a sequenced elimination-cyclopropanation process promoted by Samarium/diiodomethane or Samarium diiodide and Samarium/diiodomethane.
Sequential Elimination−Cyclopropanation Reactions Promoted by Samarium: Highly Diastereoselective Synthesis of Cyclopropylamides
摘要:
trans-Cyclopropanamides were obtained, in high yield, from 2-chloro-3-hydroxyamides by a sequenced elimination-cyclopropanation process promoted by Samarium/diiodomethane or Samarium diiodide and Samarium/diiodomethane.
Sequential Elimination−Cyclopropanation Reactions Promoted by Samarium: Highly Diastereoselective Synthesis of Cyclopropylamides
作者:José M. Concellón、Humberto Rodríguez-Solla、Ricardo Llavona
DOI:10.1021/jo0262098
日期:2003.2.1
trans-Cyclopropanamides were obtained, in high yield, from 2-chloro-3-hydroxyamides by a sequenced elimination-cyclopropanation process promoted by Samarium/diiodomethane or Samarium diiodide and Samarium/diiodomethane.