化学
加合物
分子内力
环加成
烷基化
Diels-Alder反应
立体化学
有机化学
催化作用
作者
Siyuan Luo,Zhuo-Ya Tang,Qingjiang Li,Jiang Weng,Sheng Yin,Gui‐Hua Tang
标识
DOI:10.1021/acs.joc.1c00229
摘要
Mulberry Diels–Alder-type adducts (MDAAs) are a group of rare natural polyphenols biosynthetically derived from [4 + 2]-cycloaddition of chalcones and dehydroprenylphenols. In this study, kuwanons G (1) and H (2), two bioactive MDAAs with unique dehydroprenylflavonoid dienes, were totally synthesized for the first time in a biomimetic manner. The key features of the convergent route include the use of the Baker–Venkataraman rearrangement, alkylation of β-diketone, intramolecular cyclization, and Suzuki–Miyaura coupling to achieve the subunit diene.
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