氨基叠氮参和的Schmidt反应和(±)-amtofine的合成研究.pdf

氨基叠氮参和的Schmidt反应和(±)-amtofine的合成研究.pdf

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Abstract ThisthesisfocusedontheSchmidtreactionof twocentral azides,and contentswereincluded:f1) alkyl Schmidtreaction ofaromatic withanazido ofSchmidtreactionof aldehydes amine,and(2)design acyl chlorideswith azidesandits inthe ontotal ofantofme.Inthefirst alkyl applicationattempt synthesis part, theexclusive wasobservedintheSchmidt 1.2-aryl reactionofaromatic with3. migration aldehydes theformalmetal—free ofaromaticwasachieved azido-N-tosylpropan-1·amine,thenN-arylation aldehydes Inthesecond substrateoftheintramolecularSchmidt part,the reactionof chlorideswas acyl designed. and ofmethinewascontrolled.Thenthe ion migration wasobtainedasintermediate group n-acyliminium andwas insituthearomatictobenzoindolizidine.Theconversion capturedby ring was tothe employed onthetotal ofantofine. attempt synthesis In a fullreviewontheSchmidtreactionof andits in chapter1,wepresented aldehydesapplication ofnatural synthesis products. In andrealization Schmidtreaction is chapter2,thedesign described. ofaryl-migration ofarylaldehyde Theexclusive ofan over was theformal migrationaryl observed,with of

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