Research output: Contribution to journal › Article › peer-review
A facile tandem carbene-ylide route to 2-fluoropyrrole derivatives. / Novikov, Mikhail S.; Khlebnikov, Alexander F.; Sidorina, Elena S.; Kostikov, Rafael R.
In: Journal of Fluorine Chemistry, Vol. 90, No. 2, 20.07.1998, p. 117-119.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - A facile tandem carbene-ylide route to 2-fluoropyrrole derivatives
AU - Novikov, Mikhail S.
AU - Khlebnikov, Alexander F.
AU - Sidorina, Elena S.
AU - Kostikov, Rafael R.
N1 - Funding Information: We gratefully acknowledge support from the Russian Foundation for Basic Research (grant No. 97-03-33087). Copyright: Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1998/7/20
Y1 - 1998/7/20
N2 - 2-Fluoropyrroles were synthesised via 1,3-dipolar cycloaddition of iminiodifluoromethanides derived from corresponding imines and difluorocarbene to dimethyl acetylenedicarboxylate.
AB - 2-Fluoropyrroles were synthesised via 1,3-dipolar cycloaddition of iminiodifluoromethanides derived from corresponding imines and difluorocarbene to dimethyl acetylenedicarboxylate.
KW - 2-Fluoropyrroles
KW - Azomethine ylides
KW - Cycloaddition
KW - Difluorocarbene
UR - http://www.scopus.com/inward/record.url?scp=0032551443&partnerID=8YFLogxK
U2 - 10.1016/S0022-1139(98)00160-2
DO - 10.1016/S0022-1139(98)00160-2
M3 - Article
VL - 90
SP - 117
EP - 119
JO - Journal of Fluorine Chemistry
JF - Journal of Fluorine Chemistry
SN - 0022-1139
IS - 2
ER -
ID: 5057159