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
收藏
页数:30
相关论文
共 50 条
  • [41] Recent Advances in Sustainable Total Synthesis and Chiral Pool Strategies with Emphasis on (-)-Sclareol in Natural Products Synthesis
    Selka, Ayyoub
    Abidli, Abdelnasser
    Schiavo, Lucie
    Jeanmart, Loic
    Hanquet, Gilles
    Lubell, William D.
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2025, 28 (08)
  • [42] RECENT ADVANCES IN THE SYNTHESIS AND REACTIONS OF CHIRAL ENOLATES
    EVANS, DA
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1992, 204 : 160 - ORGN
  • [43] Recent advances in the synthesis of naturally occurring polyhydroxylated alkaloids
    Yoda, H
    CURRENT ORGANIC CHEMISTRY, 2002, 6 (03) : 223 - 243
  • [44] Recent Advances in Lamellarin Alkaloids: Isolation, Synthesis and Activity
    Pla, D.
    Albericio, F.
    Alvarez, M.
    ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2008, 8 (07) : 746 - 760
  • [45] Novel synthesis of the natural protoberberine alkaloids: Oxypalmatine and oxypseudopalmatine
    Le, Thanh Nguyen
    Cho, Won-Jea
    BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2007, 28 (05): : 763 - 766
  • [46] Recent Advances of Transition Metal-Mediated Oxidative Radical Reactions in Total Synthesis of Indole Alkaloids
    Liang, Kangjiang
    Xia, Chengfeng
    CHINESE JOURNAL OF CHEMISTRY, 2017, 35 (03) : 255 - 270
  • [47] Recent Advances in the Total Synthesis of Aspidosperma and Kopsia Alkaloids Using Tetracyclic Pyridocarbazoles as Versatile Building Blocks
    Wang, Nengzhong
    Xiao, Xiao
    Liu, Cheng-Xiong
    Yao, Hui
    Huang, Nianyu
    Zou, Kun
    ADVANCED SYNTHESIS & CATALYSIS, 2022, 364 (15) : 2479 - 2501
  • [48] Recent advances in the synthesis of naturally occurring pyrrolidines, pyrrolizidines and indolizidine alkaloids using proline as a unique chiral synthon
    Bhat, Chinmay
    Tilve, Santosh G.
    RSC ADVANCES, 2014, 4 (11) : 5405 - 5452
  • [49] STUDIES PROTOBERBERINE ALKALOIDS .8. SYNTHESIS OF (+/-)-STEPHOLIDINE
    RAJESWARI, S
    SUGUNA, H
    PAI, BR
    COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 1977, 42 (07) : 2207 - 2216
  • [50] Recent advances in the synthesis of tetrahydrofurans and applications in total synthesis
    de la Torre, Aurelien
    Cuyamendous, Claire
    Bultel-Ponce, Valerie
    Durand, Thierry
    Galano, Jean-Marie
    Oger, Camille
    TETRAHEDRON, 2016, 72 (33) : 5003 - 5025