Regioselective synthesis of 3H-Pyrazoles bearing difluoromethyl phosphonate group DOI Open Access
Ita Hajdin, Romana Pajkert, Haibo Mei

и другие.

Journal of Fluorine Chemistry, Год журнала: 2023, Номер 273, С. 110218 - 110218

Опубликована: Ноя. 21, 2023

Язык: Английский

Synthesis of phosphonate-containing compounds DOI
Rahimeh Hajinasiri

Tetrahedron, Год журнала: 2023, Номер 149, С. 133708 - 133708

Опубликована: Окт. 27, 2023

Язык: Английский

Процитировано

2

Aza-Wittig reaction of (β-diazo-α,α-difluoroethyl)phosphonates with aldehydes for the synthesis of difluoromethylphosphonate-containing arylidene hydrazones DOI Open Access
Qian Wang, Romana Pajkert, Haibo Mei

и другие.

Journal of Fluorine Chemistry, Год журнала: 2023, Номер 273, С. 110226 - 110226

Опубликована: Ноя. 29, 2023

Язык: Английский

Процитировано

2

Catalyst-free gem-chlorosulfurization of difluoromethyl-substituted diazo compounds with disulfide and PhICl2 DOI
Jiuling Li, Bin Li, Juan Chen

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2021, Номер 19(37), С. 8030 - 8034

Опубликована: Янв. 1, 2021

A series of gem -chlorosulfurization products bearing difluoromethyl substituents were synthesized from TsCF 2 CHN , disulfides and PhICl under mild conditions, which could be efficiently converted to multi-component by a facile operation.

Язык: Английский

Процитировано

5

Cu‐Catalyzed Reaction of Trifluoromethylated β‐Keto Diazos and Nitriles Proceeding via H2O Addition to Nitrile Ylides DOI
Haibo Mei,

Youlong Du,

Qian Wang

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2024, Номер 366(16), С. 3443 - 3449

Опубликована: Май 22, 2024

Abstract A Cu‐catalyzed multi‐component reaction of trifluoromethylated β‐amino ketones and nitriles using tert ‐butyl nitrite as a diazotization reagent has been developed. Under the optimized conditions, N ‐trifluoroalkyl amides were obtained with yields up to 87%. Control experiments computational studies reveal that proceeds through generation diazo, in situ formation nitrile ylide, water addition final enol tautomerism. This approach features mild wide substrate tolerance, scale‐up applicability, which provides an efficient practical strategy for amide synthesis.

Язык: Английский

Процитировано

0

Regioselective synthesis of 3H-Pyrazoles bearing difluoromethyl phosphonate group DOI Open Access
Ita Hajdin, Romana Pajkert, Haibo Mei

и другие.

Journal of Fluorine Chemistry, Год журнала: 2023, Номер 273, С. 110218 - 110218

Опубликована: Ноя. 21, 2023

Язык: Английский

Процитировано

1