Recent advances in total synthesis of protoberberine and chiral tetrahydroberberine alkaloids

被引:3
|
作者
Niu, Zhen-Xi [1 ]
Wang, Ya-Tao [2 ,4 ]
Wang, Jun-Feng [3 ]
机构
[1] Zhengzhou Univ, Childrens Hosp, Henan Childrens Hosp, Zhengzhou Childrens Hosp, Zhengzhou 450018, Peoples R China
[2] First Peoples Hosp Shangqiu, Shangqiu 476000, Henan, Peoples R China
[3] Harvard Med Sch, Massachusetts Gen Hosp, Gordon Ctr Med Imaging, 125 Nashua St,Suite 660, Boston, MA 02114 USA
[4] Jilin Univ, China Japan Union Hosp, Dept Orthoped, Changchun 130033, Peoples R China
关键词
ENANTIOSELECTIVE TOTAL-SYNTHESIS; ASYMMETRIC-SYNTHESIS; NATURAL-PRODUCT; BERBERINE DERIVATIVES; ACCESS; AGENTS; PICTET; ISOQUINOLINES; BIOSYNTHESIS; CONSTRUCTION;
D O I
10.1039/d4np00016a
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Covering: Up to 2024Due to the widespread distribution of protoberberine alkaloids (PBs) and tetrahydroberberine alkaloids (THPBs) in nature, coupled with their myriad unique physiological activities, they have garnered considerable attention from medical practitioners. Over the past few decades, synthetic chemists have devised various total synthesis methods to attain these structures, continually expanding reaction pathways to achieve more efficient synthetic strategies. Simultaneously, the chiral construction of THPBs has become a focal point. In this comprehensive review, we categorically summarized the developmental trajectory of the total synthesis of these alkaloids based on the core closure strategies of protoberberine and tetrahydroberberine. In this comprehensive review, we categorically summarized the developmental trajectory of the total synthesis of these alkaloids based on the core closure strategies of protoberberine and tetrahydroberberine.
引用
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页数:30
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