Reaction of methyl 1-bromocycloalkanecarboxylates with zinc and N-cyclohexyl-2-oxo- and 6-bromo-N-cyclohexyl-2-oxochromene-3-carboxamides

被引：0

作者：

N. F. Kirillov

E. A. Nikiforova

D. V. Baibarodskikh

机构：

[1] Perm State National Research University,

来源：

Russian Journal of Organic Chemistry | 2015年 / 51卷

关键词：

Lactone; Cyclopentane; Trione; Cyclobutane; Cycloalkane;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Methyl 1-bromocycloalkanecarboxylates reacted with zinc and N-cyclohexyl-2-oxo- or 6-bromo-N-cyclohexyl-2-oxochromene-3-carboxamides to give methyl 1-[3-(cyclohexylcarbamoyl)-2-oxochroman-4-yl]- or methyl 1-[6-bromo-3-(cyclohexylcarbamoyl)-2-oxochroman-4-yl]cycloalkanecarboxylates and 3-cyclohexyl- or 9-bromo-3-cyclohexylspiro[chromeno[3,4-c]pyridine-1,1′-cycloalkane]-2,4,5(3H,4aH,10bH)-triones.

引用

页码：518 / 521

页数：3

共 8 条

[1] Reformatsky reaction of methyl 1-bromocyclohexane-1-carboxylate with N-aryl-2-oxochromene-3-carboxamides
V. V. Shchepin
N. F. Kirillov
M. I. Vakhrin
O. B. Bayanova
S. N. Shurov
P. S. Silaichev
Russian Journal of General Chemistry, 2006, 76 : 1146 - 1149
[2] Reformatsky reaction of methyl 1-bromocyclohexane-1-carboxylate with N-aryl-2-oxochromene-3-carboxamides
Shchepin, V. V.
Kirillov, N. F.
Vakhrin, M. I.
Bayanova, O. B.
Shurov, S. N.
Silaichev, P. S.
RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2006, 76 (07) : 1146 - 1149
[3] Reactions of zinc enolates derived from 1-aryl-2-bromo-2-phenylethanone and 2-bromoindan-1-one with alkyl 2-oxochromene-and 6-bromo-2-oxochromene-3-carboxylates
V. V. Shchepin
A. E. Korzun
M. I. Vakhrin
P. S. Silaichev
M. A. Ezhikova
M. I. Kodess
Russian Journal of General Chemistry, 2006, 76 : 777 - 780
[4] Reactions of zinc enolates derived from 1-aryl-2-bromo-2-phenylethanone and 2-bromoindan-1-one with alkyl 2-oxochromene and 6-bromo-2-oxochromene-3-carboxylates
Shchepin, V. V.
Korzun, A. E.
Vakhrin, M. I.
Silaichev, P. S.
Ezhikova, M. A.
Kodess, M. I.
RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2006, 76 (05) : 777 - 780
[5] Study of reaction of reformatsky reagent prepared from methyl bromocyclopentanecarboxylate and zinc with 2-oxochromen-and 6-bromo-2-oxochromen-3-carboxylic acids N-arylamides
V. V. Shchepin
N. F. Kirillov
M. I. Vakhrin
O. B. Bayanova
S. N. Shurov
Russian Journal of Organic Chemistry, 2007, 43 : 1545 - 1547
[6] Study of reaction of reformatsky reagent prepared from methyl bromocyclopentanecarboxylate and zinc with 2-oxochromen- and 6-bromo-2-oxochromen-3-carboxylic acids N-arylamides
Shchepin, V. V.
Kirillov, N. F.
Vakhrin, M. I.
Bayanova, O. B.
Shurov, S. N.
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2007, 43 (10) : 1545 - 1547
[7] 6-Methyl-2-(3-methyl-5-oxo-2,5-dihydropyrazolyl)-pyrimidin-4(1H)-one as CH acid in Michael reaction
A. V. Erkin
V. I. Krutikov
Russian Journal of General Chemistry, 2009, 79 : 1525 - 1531
[8] Five-membered 2,3-dioxo heterocycles: LXXXV. Synthesis of methyl 1-aryl-4,5-dioxo-3-(1-oxo-3-phenylprop-2-en-1-yl)-4,5-dihydro-1H-pyrrole-2-carboxylates and their reaction with 3-amino-5,5-dimethylcyclohex-2-en-1-ones. Molecular and crystalline structure of 4′-hydroxy-1′-(4-methoxyphenyl)-6,6-dimethyl-3′-(1-oxo-3-phenylprop-2-en-1-yl)-1-phenyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1H,1′H,5H)-trione
P. S. Silaichev
V. O. Filimonov
P. A. Slepukhin
A. N. Maslivets
Russian Journal of Organic Chemistry, 2012, 48 : 561 - 565

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