A FACILE ENTRY TO MACROCYCLIC DISULFIDES - AN EFFICIENT SYNTHESIS OF REDOX-SWITCHED CROWN-ETHERS

被引:71
作者
RAMESHA, AR [1 ]
CHANDRASEKARAN, S [1 ]
机构
[1] INDIAN INST SCI,DEPT ORGAN CHEM,BANGALORE 560012,KARNATAKA,INDIA
关键词
D O I
10.1021/jo00085a025
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An interesting sulfur transfer reaction with benzyltriethylammonium tetrathiomolybdate has been used efficiently for the synthesis of macrocyclic disulfides. This methodology has been extended to a high-yield synthesis of ''redox-switched'' crown ethers which have potential application for selective ion transport across liquid membranes.
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页码:1354 / 1357
页数:4
相关论文
共 33 条
[31]   CONVENIENT SYNTHESIS OF 2,3,12,13-TETRATHIA[4.4]METACYCLOPHANES AND 2,3,12,13-TETRATHIA[4.4]PARACYCLOPHANES [J].
TAM, TF ;
WONG, PC ;
SIU, TW ;
CHAN, TL .
JOURNAL OF ORGANIC CHEMISTRY, 1976, 41 (07) :1289-1291
[32]   TRIAZAMACROCYCLE HAVING PYRIDINE-PENDANT ARMS AS A NEW NA+ ION-SELECTIVE IONOPHORE [J].
TSUKUBE, H ;
YAMASHITA, K ;
IWACHIDO, T ;
ZENKI, M .
TETRAHEDRON LETTERS, 1989, 30 (30) :3983-3986
[33]  
WEBBER E, 1976, CHEM BER, V10, P1803