前往化源商城

The Journal of Organic Chemistry

Cupped azacyclophanes based on a m-terphenyl framework: conformational features of their N-tosylamide precursors

TK Vinod, H Hart

文献索引:Vinod, Thottumkara K.; Hart, Harold Journal of Organic Chemistry, 1990 , vol. 55, # 20 p. 5461 - 5466

全文:HTML全文

被引用次数: 21

摘要

Tetrabromomethyl m-terphenyl4 was used to construct tetrakis-N-tosylamide cuppedophanes 8-10 and, by detosylation, the corresponding tetraazacuppedophanes 17- 19. The para-and meta-bridged tosylamides 8 and 9 are conformationally rigid, but the ortho- bridged isomer 10 is conformationally mobile. At low temperatures diagonally opposite tosylamide groups are magnetically equivalent but form two nonequivalent seta which ...