@article{oai:soar-ir.repo.nii.ac.jp:00010249, author = {Kurogome, Yuji and Kogiso, Masaya and Looi, Kok Kong and Hattori, Yasunao and Konno, Hiroyuki and Hirota, Mitsuru and Makabe, Hidefumi}, issue = {39}, journal = {TETRAHEDRON}, month = {Sep}, note = {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., Article, TETRAHEDRON. 69(39):8349-8352 (2013)}, pages = {8349--8352}, title = {Total synthesis of (+)-azimine via diastereoselective aminopalladation}, volume = {69}, year = {2013} }