Xiang-Ting Min
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Explore the profile of Xiang-Ting Min including associated specialties, affiliations and a list of published articles.
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14
Citations
40
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Recent Articles
1.
Liu H, Ji D, Min X, Mei Y, Sun S, Zhang G, et al.
Org Lett
. 2023 Mar;
25(11):1878-1882.
PMID: 36916741
The formation of one unavoidable byproduct in traditional disproportionation reactions limits their applications in synthesis. Inspired by convergent disproportionation, we develop an iodine-induced cyclization and oxidation of allylic alcohols to...
2.
Ji D, Hu Y, Min X, Liu H, Zhang W, Li Y, et al.
Angew Chem Int Ed Engl
. 2022 Nov;
62(2):e202213074.
PMID: 36372782
Skeletal reorganization reactions have emerged as an intriguing tool for converting readily available compounds into complicated molecules inaccessible by traditional methods. Herein, we report a unique skeleton-reorganizing coupling reaction of...
3.
Yang F, He G, Sun S, Song T, Min X, Ji D, et al.
J Org Chem
. 2022 Oct;
87(21):14241-14249.
PMID: 36219805
By complementing traditional transition metal catalysis, photoinduced catalysis has emerged as a versatile and sustainable way to achieve carbon-heteroatom bond formation. This work discloses a visible-light-induced reaction for the formation...
4.
Zheng H, Liu C, Guo S, He G, Min X, Zhou B, et al.
Nat Commun
. 2022 Jun;
13(1):3496.
PMID: 35715392
Metallocenes are privileged backbones for synthesis and catalysis. However, the direct dehydrogenative C-H functionalization of unsymmetric metallocenes suffers from reactivity and selectivity issues. Herein, we report an electrochemically driven regioselective...
5.
Min X, Mei Y, Chen B, He L, Song T, Ji D, et al.
J Am Chem Soc
. 2022 Jun;
144(25):11081-11087.
PMID: 35709491
The recent surge in the applications of deuterated drug candidates has rendered an urgent need for diverse deuterium labeling techniques. Herein, an efficient Rh-catalyzed deuterated Tsuji-Wilkinson decarbonylation of naturally available...
6.
Guo S, Yang F, Song T, Guan Y, Min X, Ji D, et al.
Nat Commun
. 2021 Nov;
12(1):6538.
PMID: 34764303
The Mizoroki-Heck reaction and its reductive analogue are staples of organic synthesis, but the ensuing products often lack a chemical handle for further transformation. Here we report an atom-economical cross-coupling...
7.
Guan Y, Min X, He G, Ji D, Guo S, Hu Y, et al.
iScience
. 2021 Sep;
24(9):102969.
PMID: 34466792
Ritter reaction has been recognized as an elegant strategy to construct the C-N bond. Its key feature is forming the carbocation for nucleophilic attack by nitriles. Herein, we report a...
8.
Jiang W, Ji D, Zhang W, Zhang G, Min X, Hu Y, et al.
Angew Chem Int Ed Engl
. 2021 Jan;
60(15):8321-8328.
PMID: 33463001
Depending on the reactant property and reaction mechanism, one major regioisomer can be favored in a reaction that involves multiple active sites. Herein, an orthogonal regulation of nucleophilic and electrophilic...
9.
Shen B, Min X, Hu Y, Qian L, Yang S, Wan B, et al.
Org Biomol Chem
. 2020 Nov;
18(45):9253-9260.
PMID: 33150922
A distinct copper-catalyzed boroacylation of allenes with acyl chlorides and bis(pinacolato)diboron is developed. For aromatic acyl chlorides, 1,2-boroacylation of allenes readily takes place, leading to the formation of tetrasubstituted vinylboronates...
10.
Min X, Ji D, Guan Y, Guo S, Hu Y, Wan B, et al.
Angew Chem Int Ed Engl
. 2020 Sep;
60(3):1583-1587.
PMID: 32990397
Transition metal catalyzed decarbonylation offers a distinct synthetic strategy for new chemical bond formation. However, the π-backbonding between CO π* orbitals and metal center d-orbitals impedes ligand dissociation to regenerate...