Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Shi-Chao Lu"'
Publikováno v:
Molecules, Vol 28, Iss 13, p 4888 (2023)
Pynegabine, an antiepileptic drug candidate in phase I clinical trials, is a structural analog of the marketed drug retigabine with improved chemical stability, strong efficacy, and a better safety margin. The reported shortest synthetic route for py
Externí odkaz:
https://doaj.org/article/4050ceb3f4564e51add66534b29de63f
Publikováno v:
Molecules, Vol 25, Iss 18, p 4211 (2020)
The palhinine family of Lycopodium alkaloids were first reported in 2010, which feature an intriguing isotwistane carbon cage and a nine-membered azonane ring. It is noteworthy that the tetracyclic 5/6/6/9 skeleton was unprecedented in Lycopodium alk
Externí odkaz:
https://doaj.org/article/018e1a3068d841e78c4402d01366fd2f
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 93, Iss 4, Pp 620-621 (2018)
Externí odkaz:
https://doaj.org/article/49b592edc14b478abf17942576f1e393
Publikováno v:
Organic & Biomolecular Chemistry; 5/7/2024, Vol. 22 Issue 17, p3439-3443, 5p
Publikováno v:
Synthetic Communications. 52:2198-2204
An effective method for selectively oxidizing benzylic and allylic alcohols, including those deactivated by electron-withdrawing groups, was described with hypervalent iodine (III)/catalytic DDQ under mild conditions. This reaction could be performed
Publikováno v:
Angewandte Chemie International Edition. 62
Publikováno v:
Green Chemistry. 23:8964-8968
A metal-free redox arylation of alkynes with sulfoxides has been developed to provide unconventional access to diverse γ-arylated 1,3-dicarbonyl compounds in an atom-economical manner. Mechanistic studies suggest that a conjugated allenone intermedi
Publikováno v:
RSC Advances. 10:19083-19087
An acid, transition-metal, and chromatography-free radical nitration/cyclisation of 2-alkynylthioanisoles or -selenoanisoles has been developed. This is the first example of the use of highly unstable 2-nitrovinyl radicals for C–S bond formation. T
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
Organic Chemistry Frontiers. 6:2467-2470
Mycobactin T analogue 1 (MbT-1) is a mycobacterial-specific siderophore analogue, which is usually employed to conjugate therapeutic drugs to induce selective antibacterial activity. In this article, the scalable total synthesis of MbT-1 was accompli