misc
"タイトル(日本語)","タイトル(英語)","著者(日本語)","著者(英語)","担当区分","概要(日本語)","概要(英語)","出版者・発行元(日本語)","出版者・発行元(英語)","出版年月","誌名(日本語)","誌名(英語)","巻","号","開始ページ","終了ページ","記述言語","査読の有無","招待の有無","掲載種別","国際・国内誌","国際共著","DOI","ISSN","eISSN","URL","URL2","主要な業績かどうか","公開の有無"
"Recent Advances in the Total Synthesis of Xanthanolide Sesquiterpenoids","Recent Advances in the Total Synthesis of Xanthanolide Sesquiterpenoids","Kozo Shishido","Kozo Shishido","null","null","null","null","null","2009-04-01","Heterocycles","Heterocycles","Vol.78","No.4","873","889","eng","null","null","introduction_scientific_journal","null","null","10.3987/REV-08-647","0385-5414","null","http://ci.nii.ac.jp/naid/40016499763/","null","null","null"
"アレロパシー活性セスキテルペノイド,ヘリアンヌオール類の合成","Synthetic Studies on Heliannuol Sesquiterpenoids with Allelopathic Activity","亀井 智代, 森本 幸恵, 宍戸 宏造","亀井 智代, 森本 幸恵, Kozo Shishido","null","Heliannuol sesquiterpenoids have been isolated by Macias from the extracts of cultivated sunflowers (Helianthus annuus L. SH-222) and are believed to be involved in the allelopathic action of sunflowers. The characteristic phytotoxic activity, coupled with their unique structural features, has made these terpenoids desirable targets for synthetic chemists. In this article, the total synthetic studies on heliannuol sesquiterpenoids have been reviewed mainly focusing on our experimental endeavor. In the first part, the first enantioselective total syntheses of (-) -heliannuol D and (+) -heliannuol A have been mentioned. Alternative synthesis of (+) -heliannuol D, the natural enantiomer, has also been described. In the next chapter, syntheses of optically active heliannuols A, K, G, H and L were shown. Interestingly, the structures of heliannuols G and H were revised by our total synthesis. In the last chapter, the syntheses of heliannuols E and C and determination of their absolute structures were described.","Heliannuol sesquiterpenoids have been isolated by Macias from the extracts of cultivated sunflowers (Helianthus annuus L. SH-222) and are believed to be involved in the allelopathic action of sunflowers. The characteristic phytotoxic activity, coupled with their unique structural features, has made these terpenoids desirable targets for synthetic chemists. In this article, the total synthetic studies on heliannuol sesquiterpenoids have been reviewed mainly focusing on our experimental endeavor. In the first part, the first enantioselective total syntheses of (-) -heliannuol D and (+) -heliannuol A have been mentioned. Alternative synthesis of (+) -heliannuol D, the natural enantiomer, has also been described. In the next chapter, syntheses of optically active heliannuols A, K, G, H and L were shown. Interestingly, the structures of heliannuols G and H were revised by our total synthesis. In the last chapter, the syntheses of heliannuols E and C and determination of their absolute structures were described.","null","null","2006-10-01","有機合成化学協会誌","Journal of Synthetic Organic Chemistry, Japan","Vol.64","No.10","1021","1031","jpn","null","null","introduction_scientific_journal","null","null","10.5059/yukigoseikyokaishi.64.1021","0037-9980","null","http://ci.nii.ac.jp/naid/10018311513/","null","null","null"
"生体触媒を用いる生物活性天然物の合成","生体触媒を用いる生物活性天然物の合成","宍戸 宏造","Kozo Shishido","null","null","null","null","null","2004-08","化学工業","Chemical Industry","Vol.55","No.8","623","633","null","null","null","introduction_scientific_journal","null","null","null","0451-2014","null","https://ci.nii.ac.jp/naid/40006346919/","null","null","null"