THE FIRST IRON-MEDIATED CATALYTIC CARBON-NITROGEN BOND FORMATION - [4-MONOXIDE(1] CYCLOADDITION OF ALLENYL IMINES AND CARBON)

Citation
Ms. Sigman et Be. Eaton, THE FIRST IRON-MEDIATED CATALYTIC CARBON-NITROGEN BOND FORMATION - [4-MONOXIDE(1] CYCLOADDITION OF ALLENYL IMINES AND CARBON), Journal of organic chemistry, 59(24), 1994, pp. 7488-7491
Citations number
17
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00223263
Volume
59
Issue
24
Year of publication
1994
Pages
7488 - 7491
Database
ISI
SICI code
0022-3263(1994)59:24<7488:TFICCB>2.0.ZU;2-2
Abstract
Catalytic carbon-nitrogen bond formation was achieved by iron carbonyl s in the [4 + 1] cycloaddition of allenyl imines with CO. The Fe(CO)(5 ) photochemically catalyzed reaction of allenyl imines and CO gives pr eparatively useful yields of 3-alkylidene-4-pyrrolin-2-ones. These rea ctions take place under mild conditions and only require fluorescent l ight! Good control of alkylidene bond stereochemistry is achieved when the terminal allene groups are tert-butyl and methyl. Experiments in the dark show that stoichiometric Fe-2(CO)(9) can mediate [4 + 1] asse mbly by a purely thermal reaction to give good yields of the pyrrolino ne products. These new methods for the construction of 3-alkylidene-4- pyrrolin-2-ones are complimentary to existing procedures and allow for a greater variety of alkylidene substituents.