Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Linwei Zeng"'
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-10 (2023)
Abstract Indole alkaloids are one of the largest alkaloid classes, proving valuable structural moiety in pharmaceuticals. Although methods for the synthesis of indole alkaloids are constantly explored, the direct single-step synthesis of these chemic
Externí odkaz:
https://doaj.org/article/a741aad8c47048828a3325c03fe39058
Autor:
Zhencheng Lai, Rongkai Wu, Jiaming Li, Xing Chen, Linwei Zeng, Xi Wang, Jingjing Guo, Zujin Zhao, Hironao Sajiki, Sunliang Cui
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-8 (2022)
The Mannich reaction is a three-component reaction for preparing alkylamines, but the nucleophilic components rely on C(sp2)−H and activated C(sp3)−H bonds. Here, the authors report an unprecedented multicomponent double Mannich alkylamination fo
Externí odkaz:
https://doaj.org/article/08985c6c530e46a7936d729cf47d2761
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-10 (2020)
Skeletal reorganizations are intriguing processes in chemical synthesis due to their mechanism, atom-economy and synthetic versatility. Herein, the authors describe a divergent skeletal reorganization of N-sulfonyl ynamides to thiete sulfones and pro
Externí odkaz:
https://doaj.org/article/dd9c238a04704969ba04b16577ef6e79
Publikováno v:
Chemical Science; 4/14/2024, Vol. 15 Issue 14, p5211-5217, 7p
Publikováno v:
Organic Letters. 25:443-448
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5efc4c27443c3f19c124939f7abb9f6b
https://doi.org/10.1021/acs.orglett.2c04247
https://doi.org/10.1021/acs.orglett.2c04247
Axially chiral scaffolds, namely atropisomers, are widely found in natural products, pharmaceuticals, functional materials as well as chiral catalysts and ligands. Over the past decades, the construction of axial chirality has become one of hot topic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52e5909d0cad63845f1097db41b8ff68
https://doi.org/10.26434/chemrxiv-2023-5fgvp-v2
https://doi.org/10.26434/chemrxiv-2023-5fgvp-v2
Publikováno v:
The Journal of Organic Chemistry. 87:2821-2830
A facile synthesis of γ-butenolides and maleic anhydrides via annulation of α-keto acids and triazenyl alkynes is described. In this process, α-keto acids and triazenyl alkynes could undergo a self-catalyzed annulation at room temperature to deliv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f66a4d5405ac72e9254927e11434d6e4
https://doi.org/10.1021/acs.joc.1c02727
https://doi.org/10.1021/acs.joc.1c02727
Publikováno v:
Organic Chemistry Frontiers. 9:3757-3762
A multicomponent reaction for the synthesis of β-aminoxy amides is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22bf90a223e2a8c0967745d0f821a913
https://doi.org/10.1039/d2qo00631f
https://doi.org/10.1039/d2qo00631f
Autor:
Linwei Zeng, Dinggui Luo, Lirong Liu, Xuexia Huang, Yu Liu, Lezhang Wei, Tangfu Xiao, Qihang Wu
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca38800de21397e6a03182c309dcb38
https://doi.org/10.2139/ssrn.4378250
https://doi.org/10.2139/ssrn.4378250
Autor:
Sunliang Cui, Linwei Zeng
Publikováno v:
Nature Chemistry. 15:597-598
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19a593aa7eb85c8533e130d23e6b9120
https://doi.org/10.1038/s41557-023-01182-5
https://doi.org/10.1038/s41557-023-01182-5