INDOLES .1. THE BZ-NITRO-2-3-DIMETHYLINDOLES AND THEIR USE IN PREPARING NITRO-2-AMINOACETOPHENONES

被引：36

作者：

SCHOFIELD, K

THEOBALD, RS

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY | 1949年 / APR期

关键词：

D O I：

10.1039/jr9490000796

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：796 / 799

页数：4

共 25 条

[1] BARCLAY, 1945, J CHEM SOC, P530
[2] BAUDISCH, 1916, BER DTSCH CHEM GES, V49, P2579
[3] Nitro-indole.
Bauer, H
Strauss, E
[J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1932, 65 (02): : 308 - 315
[4] GAUDION, 1947, J CHEM SOC, P1631
[5] HOLLINS, 1924, SYNTHESIS NITROGEN R, P96
[6] JACKSON, 1881, BER, V14, P885
[7] The bromination of 1-acetyl-2,3-diphenylindole
Koelsch, CF
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1944, 66 : 1983 - 1984
[8] Korczynski A, 1926, GAZZ CHIM ITAL, V56, P903
[9] CINNOLINES .1. SYNTHESIS OF AMINOACETOPHENONES AND AMINOPROPIOPHENONES
LEONARD, NJ
BOYD, SN
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1946, 11 (04) : 405 - 418
[10] Pure l-erythrulose (l-2-keto-tetrose)
Muller, H
Montigel, C
Reichstein, T
[J]. HELVETICA CHIMICA ACTA, 1937, 20 : 1468 - 1473