Cobalt-Catalyzed Dithiolation of Unactivated Alkenes with Thiols: A Facile Access to Diverse Vicinal Dithioethers DOI
Jing Shi, Qian Xiao, Jian‐Ji Zhong

и другие.

Chemical Communications, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

A simple cobalt-catalytic aerobic approach for the direct dithiolation of unactivated alkenes with thiols has been established, enabling efficient access to symmetric and unsymmetric vicinal dithioethers under mild reaction conditions.

Язык: Английский

A General Electron Donor‐Acceptor Photoactivation Using Oxime Esters Enabled Divergent Thioetherifications DOI

Maojian Lu,

Liang‐Liang Jiang,

Yueming Xu

и другие.

Chinese Journal of Chemistry, Год журнала: 2024, Номер 42(22), С. 2751 - 2756

Опубликована: Июль 12, 2024

Comprehensive Summary The EDA complex‐mediated reactions involving oxime esters have been few studied. Herein, an complex formed by thiophenolate anion and ester is reported for photoinduced divergent synthesis of thioethers, depending on different types esters. Operational simplicity, mild reaction conditions, flexible options leaving group demonstrate the generality synthetic utility this approach. Such approach can also enable interesting thiol‐catalysis phenanthridines.

Язык: Английский

Процитировано

4

Hydropersulfide (RSSH)-Mediated Hydrothiolation of Alkenes DOI

Jeffrey Ash,

Kevin Curtis,

Shishir Bhowmik

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Янв. 3, 2025

A hydropersulfide-mediated hydrothiolation reaction of alkenes has been developed for C-S bond formation with Markovnikov selectivity. This new approach is a transition-metal-, additive-, and solvent-free under mild conditions. The postulated to proceed by an ionic mechanism the release elemental sulfur based on our control experiments density functional theory calculations.

Язык: Английский

Процитировано

0

Synergistic Enhancement of Ligand & Cluster Connectivity to Construct Highly Stable Fluorescein‐Based MOFs with Thickened Channel Walls for Boosting Photocatalytic Activity DOI Open Access

Han‐Shu Li,

Ruiting Zheng, Yanhong Liu

и другие.

Small, Год журнала: 2025, Номер unknown

Опубликована: Янв. 20, 2025

Abstract Fabricating visible‐light‐responsive metal−organic frameworks (MOFs) with high stability and effective catalytic functionality remains a long‐term pursuit yet great challenge. Herein, strategy of increasing ligand cluster connectivity is developed to construct highly stable fluorescein MOFs, La‐CFL, presenting new (4,8)‐connected topological structure compared Cd‐FL constructed using 6‐connected dinuclear clusters 3‐connected tritopic ligands. La 8 (CFL) 4 containers like Chinese “Ritual Wine Vessels (Jue)” resemble linear arrangements interconnected by the [La 2 (COO) ] clusters. This arrangement induces benzene rings xanthene locate on inner walls 1D channels, resulting in thicker channel that contribute enhanced stability. Consequently, La‐CFL demonstrates outstanding performance thiol–ene reactions under green LED irradiation. It exhibits 2.3 times higher efficiency than while reducing reaction time one‐fifth at 20 min. Furthermore, displays size‐selective catalysis retains full activity for cycles without degradation, an improvement over Cd‐FL's recyclability limitations.

Язык: Английский

Процитировано

0

Cobalt-catalyzed hydrothiolation of alkynes for the diverse synthesis of branched alkenyl sulfides DOI Creative Commons

Jiale Ying,

Yan Tan,

Zhan Lu

и другие.

Nature Communications, Год журнала: 2024, Номер 15(1)

Опубликована: Сен. 14, 2024

Язык: Английский

Процитировано

3

TfOH-catalyzed Markovnikov-selective hydrothiolation of tri- and tetrasubstituted alkenes DOI
Takanori Shibata,

Ryo Tokutake,

Mamoru Ito

и другие.

Tetrahedron Letters, Год журнала: 2025, Номер 160, С. 155550 - 155550

Опубликована: Март 30, 2025

Язык: Английский

Процитировано

0

Photocatalytic Iminothiolation of Alkenes via Monothiocarbonate Oxime Esters DOI
Ranjini Laskar,

Rebecca E. Thielemann,

Janosch Knüppe

и другие.

ACS Catalysis, Год журнала: 2025, Номер unknown, С. 6731 - 6738

Опубликована: Апрель 10, 2025

Язык: Английский

Процитировано

0

Catalytic hydrofunctionalizations of alkenes via hydrogen atom transfer with 3d transition metal complexes (MHAT): A pragmatic approach to recent contributions DOI Creative Commons
Antonio Torres-Calis, Juventino J. Garcı́a

Applied Catalysis A General, Год журнала: 2025, Номер unknown, С. 120379 - 120379

Опубликована: Май 1, 2025

Язык: Английский

Процитировано

0

The radical chemistry of N-sulfenyl phthalimides/succinimides for C S bonds formation DOI
Qian Xiao, Jian‐Ji Zhong

Tetrahedron Letters, Год журнала: 2024, Номер 144, С. 155153 - 155153

Опубликована: Июнь 17, 2024

Язык: Английский

Процитировано

2

Copper-catalyzed oxidative sulfenylation and alkylation of indolin-2-ones for direct construction of sulfur-substituted quaternary carbons DOI

Yun‐Hao Zhang,

Yinuo Wang, Ziyu Liu

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(11), С. 3131 - 3136

Опубликована: Янв. 1, 2024

A rapid and green one-pot access to S -substituted quaternary carbon centers from commercially available feedstock chemicals has been established, providing complex molecules with high chemoselectivity by the use of air as terminal oxidant.

Язык: Английский

Процитировано

1

Facile synthesis of β‐trifluoromethyl thioethers via DBN‐catalyzed hydrothiolation of a‐trifluoromethyl styrenes with thiols DOI

Yupian Deng,

Jia‐Qi Huang,

Yuhao Qian

и другие.

Chemistry - An Asian Journal, Год журнала: 2024, Номер 19(20)

Опубликована: Июль 23, 2024

Abstract A very simple and atom‐economical method for the synthesis of vicinal trifluoromethyl thioethers via DBN‐catalyzed hydrothiolation α‐(trifluoromethyl)styrenes with thiols was reported. The reaction proceeded smoothly under mild conditions provided β‐CF 3 ‐thioethers in moderate to good yields an anti‐Markovnikov manner. Furthermore, this features several remarkable advantages, such as use a catalytic amount DBN, broad substrate scope, excellent functional group compatibility, easy scalability.

Язык: Английский

Процитировано

1