- Stereoselective synthesis of a novel chiral piperazine.
[作者:Kojima, Satoshi;Chabayashi, Takashi;Umeda, Yasuhiro;Iwamoto, Akihisa;Tanabe, Kazuhisa;Ohkata, Katsuo;,期刊:Heterocycles, 页码:1493-1501 , 文章类型: 研究论文,,卷期:2008年75-6]
- (2S,6S)-2,4,6-Tris(phenylmethyl)piperazine was prepd. in 11 steps and 53% overall yield from S-phenylalanine. Key steps in the synthesis involved reductive amination to introduce an ethoxycarbonylmethyl group on to the ...
- Synthesis of the diazatricyclic core of madangamines via cyclic N,O-acetalization-bridgehead reduction.
[作者:Yoshimura, Yuta;Kusanagi, Takahiko;Kibayashi, Chihiro;Yamazaki, Naoki;Aoyagi, Sakae;,期刊:Heterocycles, 页码:1329-1354 , 文章类型: 研究论文,,卷期:2008年75-6]
- Compounds (More Than One Hetero Atom)) Section An approach to synthesize the diazatricyclic core of the madangamine alkaloids is described. The synthesis involves intramol. N,O-acetalization of the keto-aminophenol whic...
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