UNEXPECTED HYDANTOIN FORMATION IN THE ATTEMPTED AMIDATION WITH 2-AMINOBENZOPHENONE OF GLYOXYLIC-ACID USING DICYCLOHEXYLCARBODIIMIDE

被引：3

作者：

BRINGMANN, G ^{[1
]}

MADER, T ^{[1
]}

PETERS, K ^{[1
]}

VONSCHNERING, HG ^{[1
]}

机构：

[1] MAX PLANCK INST FESTKORPERFORSCH,W-7000 STUTTGART 80,GERMANY

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1993年 / 12期

关键词：

D O I：

10.1039/c39930001001

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The formation and structure elucidation of the hydantoin 5, an unexpected product from 2-aminobenzophenone 1, glyoxylic acid 2 and dicyclohexylcarbodiimide 3, is described.

引用

页码：1001 / 1002

页数：2

共 2 条

[1] UNEXPECTED FORMATION OF CONDENSED TRICYCLIC ISOSYDNONES IN REACTION OF 2-AMINOBENZOPHENONE ANTI-PHENYLSEMICARBAZONES WITH PHOSGENE
ANDRONATI, SA
YAVORSKII, AS
SIMONOV, YA
PAVLOVSKII, VI
DVORKIN, AA
CHUMAKOV, YM
ZHURNAL ORGANICHESKOI KHIMII, 1993, 29 (08): : 1582 - 1587
[2] Efficient synthesis of 2,3-dihydroquinazolin-4(1H)-ones using heterogeneous solid acid catalysts: unexpected formation of 2,3-dihydro-2-(4-(tetrahydro-2H-pyran-2-yloxy)butyl)quinazolin-4(1H)-one
Bharate, Sandip B.
Mupparapu, Nagaraju
Manda, Sudhakar
Bharate, Jaideep B.
Mudududdla, Ramesh
Yadav, Rammohan R.
Vishwakarma, Ram A.
ARKIVOC, 2012, : 308 - 318

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