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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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