Total synthesis of (+/-)-pallavicinin and (+/-)-neopallavicinin
Publication in refereed journal

替代計量分析
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其它資訊
摘要Through a biomimetic pathway, (+/-)-pallavicinin and (+/-)-neopallavicinin were synthesized from (+/-)-Wieland-Miescher ketone via Grob fragmentation, intramolecular aldol cyclization, and intramolecular Michael reaction. The synthesis was stereocontrolled efficiently and followed the stereochemistry of the Wieland-Miescher ketone, and could provide opportunities for access to analogues of pallavicinin, neopallavicinin, and other related bioactive diterpenoids.
著者Peng XS, Wong HNC
期刊名稱Chemistry - An Asian Journal
出版年份2006
月份7
日期17
卷號1
期次1-2
出版社WILEY-V C H VERLAG GMBH
頁次111 - 120
國際標準期刊號1861-4728
電子國際標準期刊號1861-471X
語言英式英語
關鍵詞aldol reaction, biomimetic synthesis, diterpenoids, labdanes, total synthesis
Web of Science 學科類別Chemistry; Chemistry, Multidisciplinary; CHEMISTRY, MULTIDISCIPLINARY

上次更新時間 2021-15-06 於 00:31