VILSMEIER-HAACK REACTION WITH SUCCINAMIDALS - A CONVENIENT SYNTHESIS OF 5-CHLOROPYRROLE-2-CARBOXALDEHYDES AND 5-CHLOROPYRROLE-2,4-DICARBOXALDEHYDES

被引：19

作者：

GUZMAN, A

ROMERO, M

MUCHOWSKI, JM

机构：

[1] SYNTEX SA,DIV INVEST,APARTADO POSTAL 10-820,MEXICO CITY 10,DF,MEXICO

[2] SYNTEX INC,INST ORGAN CHEM,PALO ALTO,CA 94304

来源：

CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE | 1990年 / 68卷 / 05期

关键词：

D O I：

10.1139/v90-125

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：791 / 794

页数：4

共 33 条

[21] VILSMEIER-HAACK REAGENT - A FACILE SYNTHESIS OF 4-HETEROMETHYLENE-2-ARYL-2-OXAZOLIN-5-ONES FROM N-ACYL-ALPHA-AMINO ACID-ESTERS
SINGH, KK
SINGH, RM
INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 1994, 33 (03): : 232 - 235
[22] Vilsmeier-Haack reaction of 7-acetyl-2-arylindoles: a convenient method for the synthesis of 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes
Mphahlele, Malose J.
Mmonwa, Mmakwena M.
ORGANIC & BIOMOLECULAR CHEMISTRY, 2019, 17 (08) : 2204 - 2211
[23] Vilsmeier-Haack reaction of 7-acetyl-2-arylindoles: a convenient method for the synthesis of 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes
Mphahlele M.J.
Mmonwa M.M.
Organic and Biomolecular Chemistry, 2019, 17 (08): : 2204 - 2211
[24] THE VILSMEIER-HAACK REACTION WITH 3,4-DISUBSTITUTED ISOXAZOLIN-5-ONES - A NEW SYNTHESIS OF 1,3-OXAZIN-6-ONES AND 1,3-OXAZINE-2,6-DIONES
BECCALLI, EM
MARCHESINI, A
MOLINARI, H
TETRAHEDRON LETTERS, 1986, 27 (05) : 627 - 630
[25] STUDIES ON VILSMEIER-HAACK REACTION - A VERSATILE NEW SYNTHESIS OF 5-CHLORO-3-METHYLPYRAZOLE-4-CARBOXALDEHYDE, 5-CHLORO-3-METHYL-1-PHENYLPYRAZOLE-4-CARBOXALDEHYDE AND RELATED FUSED HETEROCYCLIC-COMPOUNDS AND HETEROCYCLIC SCHIFFS BASES
PAWAR, RA
PATIL, AA
INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 1994, 33 (02): : 156 - 158
[26] SYNTHESIS OF 2 AMIDINE DERIVATIVES BY VILSMEIER-HAACK REACTION OF 3-AMINO-4-(H-3)-OXO-2(H-1)-PYRIMIDINETHIONE AND THEIR CONVERSION INTO 5H-1,3,4-THIADIAZOLO[3,2-ALPHA]PYRIMIDIN-5-ONES
TSUJI, T
CHEMICAL & PHARMACEUTICAL BULLETIN, 1974, 22 (02) : 471 - 472
[27] ELECTROPHILIC SUBSTITUTIONS IN 5-MEMBERED RINGS .14. MECHANISM OF VILSMEIER-HAACK REACTION .2. KINETIC STUDY OF FORMYLATION OF THIOPHENE DERIVATIVES WITH DIMETHYLFORMAMIDE AND PHOSPHORUS OXYCHLORIDE OR CARBONYL CHLORIDE IN 1,2-DICHLOROETHANE
ALUNNI, S
SANTINI, S
SAVELLI, G
MARINO, G
LINDA, P
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1972, (14): : 2070 - &
[28] 5H-furan-2-one in the Vilsmeier-Haack reaction.: Synthesis of β-substituted furans.: Molecular structures of 3-dimethylaminomethylene-5-formyl-3H-furan-2-one and dimethylammonium 3,5-di(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidenemethyl)furan-2-olate
Krapivin, GD
Kozhina, ND
Chernousenko, LA
Zavodnik, VE
KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII, 1999, (01): : 24 - 34
[29] STEROIDES HALOGENES ET INSATURES EN 3 .2. ESSAIS DE DESHALOGENATION DANS LA SERIE 5ALPHA ET PREPARATION DE NOUVEAUX DERIVES PAR EXTENSION DE LA REACTION DE VILSMEIER-HAACK ( SERIES 5ALPHA ET 5BETA )
SCHMITT, J
PANOUSE, JJ
CORNU, PJ
PLUCHET, H
HALLOT, A
COMOY, P
BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE, 1964, (11): : 2760 - &
[30] Reaction between enaminones and acetylenic esters in the presence of triphenylphosphine: a convenient synthesis of alkyl 2(1-benzyl-2,4-dioxo-2,3,4,5,6,7-hexahydro-1H-indol-3-yl)acetates
Farough Nasiri
Massood Bayzidi
Amin Zolali
Molecular Diversity, 2012, 16 : 619 - 623

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