Title of article :
Total synthesis of (+)-azimine via diastereoselective aminopalladation
Author/Authors :
Yuji Kurogome، نويسنده , , Masaya Kogiso، نويسنده , , Kok Kong Looi، نويسنده , , Yasunao Hattori، نويسنده , , Hiroyuki Konno، نويسنده , , Mitsuru Hirota، نويسنده , , Hidefumi Makabe، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
4
From page :
8349
To page :
8352
Abstract :
The aminopalladation of amino allylic alcohol using Cl2Pd(MeCN)2 in CH2Cl2 gave the 2,6-disubstituted piperidine with excellent diastereoselectivity. This compound was successfully converted into (+)-azimine (1) using cross-metathesis and Shiina macrolactonization.
Keywords :
Aminopalladation , Alkaloids , piperidine , Natural product
Journal title :
Tetrahedron
Serial Year :
2013
Journal title :
Tetrahedron
Record number :
1106266
Link To Document :
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