TY - JOUR
T1 - Scandium-catalyzed tandem selective oxirane ring-opening/Friedel-Crafts alkylation
T2 - A facile access to [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines
AU - Wei, Lai
AU - Liu, Lu
AU - Zhang, Junliang
PY - 2014/9/21
Y1 - 2014/9/21
N2 - A facile technique involving a novel Lewis-acid-catalyzed tandem selective ring-opening of oxirane and Friedel-Crafts alkylation of 1H-indol-1-yl derived oxiranes was developed. The developed protocol affords functionalized [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines in up to 95% yield. This journal is
AB - A facile technique involving a novel Lewis-acid-catalyzed tandem selective ring-opening of oxirane and Friedel-Crafts alkylation of 1H-indol-1-yl derived oxiranes was developed. The developed protocol affords functionalized [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines in up to 95% yield. This journal is
UR - https://www.scopus.com/pages/publications/84906233885
U2 - 10.1039/c4ob01057d
DO - 10.1039/c4ob01057d
M3 - 文章
C2 - 25053291
AN - SCOPUS:84906233885
SN - 1477-0520
VL - 12
SP - 6869
EP - 6877
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
IS - 35
ER -