Standard
Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives. / Kachalkina, Svetlana G.; Borodkin, Gennady S.; Pozharskii, Alexander F.; Antonov, Alexander S.; Borodkina, Inna G.; Maltsev, Yuri F.; Filatova, Ekaterina A.; Filarowski, Aleksander; Ozeryanskii, Valery A.
в:
Mendeleev Communications , Том 25, № 3, 1107, 12.06.2015, стр. 182-184.
Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Harvard
Kachalkina, SG, Borodkin, GS, Pozharskii, AF
, Antonov, AS, Borodkina, IG, Maltsev, YF, Filatova, EA, Filarowski, A & Ozeryanskii, VA 2015, '
Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives',
Mendeleev Communications , Том. 25, № 3, 1107, стр. 182-184.
https://doi.org/10.1016/j.mencom.2015.05.007APA
Kachalkina, S. G., Borodkin, G. S., Pozharskii, A. F.
, Antonov, A. S., Borodkina, I. G., Maltsev, Y. F., Filatova, E. A., Filarowski, A., & Ozeryanskii, V. A. (2015).
Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives.
Mendeleev Communications ,
25(3), 182-184. [1107].
https://doi.org/10.1016/j.mencom.2015.05.007Vancouver
Author
Kachalkina, Svetlana G. ; Borodkin, Gennady S. ; Pozharskii, Alexander F.
; Antonov, Alexander S. ; Borodkina, Inna G. ; Maltsev, Yuri F. ; Filatova, Ekaterina A. ; Filarowski, Aleksander ; Ozeryanskii, Valery A. /
Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives. в:
Mendeleev Communications . 2015 ; Том 25, № 3. стр. 182-184.
BibTeX
@article{5eb4379d357f4cc194deaa1e58f1f261,
title = "Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives",
abstract = "1,8-Bis(dimethylamino)naphthalenes bearing 2-positioned trifluoroacetyl or ethoxycarbonyl group on treatment with 2-lithio-1,8-bis-dimethylamino)naphthalene undergo base-promoted transformation into benzo[g]indole derivatives in small to moderate yield, representing previously unknown mode of the pyrrole ring closure which proceeds via deprotonation of the NMe group.",
author = "Kachalkina, {Svetlana G.} and Borodkin, {Gennady S.} and Pozharskii, {Alexander F.} and Antonov, {Alexander S.} and Borodkina, {Inna G.} and Maltsev, {Yuri F.} and Filatova, {Ekaterina A.} and Aleksander Filarowski and Ozeryanskii, {Valery A.}",
year = "2015",
month = jun,
day = "12",
doi = "10.1016/j.mencom.2015.05.007",
language = "English",
volume = "25",
pages = "182--184",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "3",
}
RIS
TY - JOUR
T1 - Base-promoted transformation of 2-C(O)R-1,8-bis(dimethylamino)naphthalenes into benzo[g]indole derivatives
AU - Kachalkina, Svetlana G.
AU - Borodkin, Gennady S.
AU - Pozharskii, Alexander F.
AU - Antonov, Alexander S.
AU - Borodkina, Inna G.
AU - Maltsev, Yuri F.
AU - Filatova, Ekaterina A.
AU - Filarowski, Aleksander
AU - Ozeryanskii, Valery A.
PY - 2015/6/12
Y1 - 2015/6/12
N2 - 1,8-Bis(dimethylamino)naphthalenes bearing 2-positioned trifluoroacetyl or ethoxycarbonyl group on treatment with 2-lithio-1,8-bis-dimethylamino)naphthalene undergo base-promoted transformation into benzo[g]indole derivatives in small to moderate yield, representing previously unknown mode of the pyrrole ring closure which proceeds via deprotonation of the NMe group.
AB - 1,8-Bis(dimethylamino)naphthalenes bearing 2-positioned trifluoroacetyl or ethoxycarbonyl group on treatment with 2-lithio-1,8-bis-dimethylamino)naphthalene undergo base-promoted transformation into benzo[g]indole derivatives in small to moderate yield, representing previously unknown mode of the pyrrole ring closure which proceeds via deprotonation of the NMe group.
UR - http://www.scopus.com/inward/record.url?scp=84930946598&partnerID=8YFLogxK
U2 - 10.1016/j.mencom.2015.05.007
DO - 10.1016/j.mencom.2015.05.007
M3 - Article
AN - SCOPUS:84930946598
VL - 25
SP - 182
EP - 184
JO - Mendeleev Communications
JF - Mendeleev Communications
SN - 0959-9436
IS - 3
M1 - 1107
ER -
