Transition-Metal-Catalyzed Transformations for the Synthesis of Marine Drugs

被引:1
作者
Parte, Lucia G. [1 ]
Fernandez, Sergio [2 ]
Sandonis, Eva [1 ]
Guerra, Javier [1 ]
Lopez, Enol [3 ]
机构
[1] Univ Valladolid UVa, Sci Fac, Dept Organ Chem, Paseo Belen 7, Valladolid 47011, Spain
[2] Queen Mary Univ London QMUL, Sch Phys & Chem Sci, Dept Chem, Mile End Rd, London E1 4NS, England
[3] Univ Valladolid UVa, Sch Engn EII, Dept Organ Chem, ITAP, Valladolid 47002, Spain
关键词
transition metals; catalytic transformations; marine drugs; bioactive molecules; CROSS-COUPLING REACTIONS; CARBON BOND FORMATION; ENANTIOSELECTIVE TOTAL-SYNTHESIS; ASYMMETRIC TOTAL-SYNTHESIS; 1ST TOTAL SYNTHESIS; NATURAL-PRODUCTS; GRIGNARD-REAGENTS; OLEFIN METATHESIS; C-C; ARENASTATIN-A;
D O I
10.3390/md22060253
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Transition metal catalysis has contributed to the discovery of novel methodologies and the preparation of natural products, as well as new chances to increase the chemical space in drug discovery programs. In the case of marine drugs, this strategy has been used to achieve selective, sustainable and efficient transformations, which cannot be obtained otherwise. In this perspective, we aim to showcase how a variety of transition metals have provided fruitful couplings in a wide variety of marine drug-like scaffolds over the past few years, by accelerating the production of these valuable molecules.
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页数:47
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