QUARARIBEA METABOLITES .3. TOTAL SYNTHESIS OF (+ -)-FUNEBRAL, A ROTATIONALLY RESTRICTED PYRROLE ALKALOID, USING A NOVEL PAAL-KNORR REACTION/

Authors
Citation
Sx. Yu et Pw. Lequesne, QUARARIBEA METABOLITES .3. TOTAL SYNTHESIS OF (+ -)-FUNEBRAL, A ROTATIONALLY RESTRICTED PYRROLE ALKALOID, USING A NOVEL PAAL-KNORR REACTION/, Tetrahedron letters, 36(35), 1995, pp. 6205-6208
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
36
Issue
35
Year of publication
1995
Pages
6205 - 6208
Database
ISI
SICI code
0040-4039(1995)36:35<6205:QM.TSO>2.0.ZU;2-B
Abstract
The total synthesis of (+/-)-funebral 5, a sterically crowded, rotatio nally restricted pyrrole alkaloid, has been achieved by means of a new variation of the Paal-Knorr synthesis, employing titanium isopropoxid e.