A new source of 1,2-dehydro-O-carborane

被引:26
作者
Atkins, JH [1 ]
Ho, DM [1 ]
Jones, M [1 ]
机构
[1] PRINCETON UNIV,DEPT CHEM,PRINCETON,NJ 08544
关键词
D O I
10.1016/0040-4039(96)01623-1
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
1,2-Dehydro-o-carborane adds to naphthalene and benzene to give Diels-Alder adducts. Treatment of the benzene adduct at 230-260 degrees C in the presence of accepters leads to transfer of 1,2-dehydro-o-carborane. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:7217 / 7220
页数:4
相关论文
共 11 条
[1]  
[Anonymous], 1994, SIEM XSCANS
[2]   REACTIONS OF 1,2-DEHYDRO-ORTHO-CARBORANE WITH DIENES [J].
GHOSH, T ;
GINGRICH, HL ;
KAM, CK ;
MOBRAATEN, EC ;
JONES, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (04) :1313-1318
[3]   CARBORANYLCARBENES AND DEHYDROCARBORANES [J].
GINGRICH, HL ;
GHOSH, T ;
HUANG, QR ;
LI, J ;
JONES, M .
PURE AND APPLIED CHEMISTRY, 1993, 65 (01) :65-71
[4]  
Grimes R, 1970, CARBORANES
[5]   ENE REACTIONS OF 1,2-DEHYDRO-ORTHO-CARBORANE [J].
HUANG, QR ;
GINGRICH, HL ;
JONES, M .
INORGANIC CHEMISTRY, 1991, 30 (17) :3254-3257
[6]  
MOBRAATEN EC, 1991, THESIS PRINCETON U
[7]  
Muetterties E. L., 1975, Boron Hydride Chemistry
[8]  
Olah G. A., 1987, Hypercarbon Chemistry
[9]  
ONAK T, 1975, CHEM REV 1992, V92, P209
[10]  
SHELDRICK G, 1993, SHELXL 93