Synthesis of 1, 3, 3-trinitroazetidine
T Axenrod, C Watnick, H Yazdekhasti, PR Dave
Index: Axenrod, Theodore; Watnick, Clara; Yazdekhasti, Hamid; Dave, Paritosh R. Tetrahedron Letters, 1993 , vol. 34, # 42 p. 6677 - 6680
Full Text: HTML
Citation Number: 38
Abstract
Abstract The t-butyldimethylsilyl ether of 3-(p-toluenesulfonamido) propane-2-ol-1-(p- toluenesulfonate) on treatment with LiH undergoes ring closure to the correponding azetidine which is readily converted to N-tosyl-3-azetidinone oxime. By oxidative nitrolysis the latter affords 1, 3, 3-trinitroazetidine.
Related Articles:
[Axenrod, T.; Watnick, C.; Yazdekhasti, H.; Dave, P. R. Journal of Organic Chemistry, 1995 , vol. 60, # 7 p. 1959 - 1964]
[Axenrod, T.; Watnick, C.; Yazdekhasti, H.; Dave, P. R. Journal of Organic Chemistry, 1995 , vol. 60, # 7 p. 1959 - 1964]