Excellent exo/endo-selectivity in the 1,3-dipolar cycloaddition of cyclic azomethine ylide: exploring the facile investigation of cocaine antagonists
| Title | Excellent exo/endo-selectivity in the 1,3-dipolar cycloaddition of cyclic azomethine ylide: exploring the facile investigation of cocaine antagonists |
| Publication Type | Journal Article |
| Year of Publication | 2007 |
| Authors | Laha, JK |
| Journal | Letters in Organic Chemistry |
| Volume | 4 |
| Start Page | JAN |
| Issue | 8 |
| Pagination | 550-552 |
| Date Published | JAN |
| Type of Article | Article |
| ISSN | 1570-1786 |
| Keywords | 1, 3-dipolar cycloaddition, cocaine antagonists, cyclic azomethine ylide, exo/endo-selectivity., tropane |
| Abstract | High exo-selectivity was achieved in the 1,3-dipolar cycloaddition of a cyclic azomethine ylide and phenyl vinyl sulfone or Opplozer's camphorsultam chiral dipolarophile leading to the synthesis of two novel tropane compounds. |
| DOI | 10.2174/157017807782795448 |
| Type of Journal (Indian or Foreign) | Foreign |
| Impact Factor (IF) | 0.756 |
Divison category:
Organic Chemistry