TY - JOUR
T1 - Copper-catalyzed transformation of carbonyl-ene-nitrile compounds
T2 - Vinylation, imino ene reaction, and alkynylation of 2-aza-2,4-cyclopentadienone intermediates generated via Ritter-type hydration and dehydrative cyclization reactions
AU - Murai, Masahito
AU - Kawai, Shigekazu
AU - Miki, Koji
AU - Ohe, Kouichi
PY - 2007/1/1
Y1 - 2007/1/1
N2 - 1H-pyrrolin-2(5H)-one derivatives are easily obtained from carbonyl-ene-nitrile compounds and alkenes or alkynes by copper(II)-catalyzed tandem sequence involving vinylation or allylation as well as Ritter-type hydration and dehydrative cyclization.
AB - 1H-pyrrolin-2(5H)-one derivatives are easily obtained from carbonyl-ene-nitrile compounds and alkenes or alkynes by copper(II)-catalyzed tandem sequence involving vinylation or allylation as well as Ritter-type hydration and dehydrative cyclization.
KW - Allylation
KW - Azacyclopentadienone
KW - Carbonyl-ene-nitrile
KW - Copper(II)-catalysis
KW - Pyrrolinone
KW - Vinylation
UR - http://www.scopus.com/inward/record.url?scp=33845625717&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33845625717&partnerID=8YFLogxK
U2 - 10.1016/j.jorganchem.2006.04.053
DO - 10.1016/j.jorganchem.2006.04.053
M3 - Article
AN - SCOPUS:33845625717
SN - 0022-328X
VL - 692
SP - 579
EP - 584
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
IS - 1-3
ER -