Three‐Component Reaction of Potassium Alkyltrifluoroborates, Sulfur Dioxide and Allylic Bromides under Visible‐Light Irradiation DOI
S. Ye, Xiaofang Li,

Wenlin Xie

и другие.

Asian Journal of Organic Chemistry, Год журнала: 2019, Номер 8(6), С. 893 - 898

Опубликована: Март 19, 2019

Abstract Diverse allylic sulfones are generated through a three‐component reaction of potassium alkyltrifluoroborates, sulfur dioxide and bromides in the presence 9‐mesityl‐10‐methyl acridinium perchlorate under visible light irradiation at room temperature. This transformation proceeds efficiently, broad scope is demonstrated with good functional groups tolerance. initiated by treatment alkyltrifluoroborate visible‐light photocatalyst, leading to alkyl radical. radical intermediate trapped provide alkylsulfonyl radical, which then undergoes further afford corresponding sulfone.

Язык: Английский

Metal-free C3-alkoxycarbonylation of quinoxalin-2(1H)-ones with carbazates as ecofriendly ester sources DOI
Long‐Yong Xie, Sha Peng,

Tai‐Gang Fan

и другие.

Science China Chemistry, Год журнала: 2019, Номер 62(4), С. 460 - 464

Опубликована: Март 7, 2019

Язык: Английский

Процитировано

124

The concept of dual roles design in clean organic preparation DOI
Zhong Cao, Qin Zhu, Ying‐Wu Lin

и другие.

Chinese Chemical Letters, Год журнала: 2019, Номер 30(12), С. 2132 - 2138

Опубликована: Сен. 19, 2019

Язык: Английский

Процитировано

123

Natural Deep Eutectic Solvent-Catalyzed Selenocyanation of Activated Alkynes via an Intermolecular H-Bonding Activation Process DOI
Chao Wu,

Haijing Xiao,

Shuwen Wang

и другие.

ACS Sustainable Chemistry & Engineering, Год журнала: 2019, Номер 7(2), С. 2169 - 2175

Опубликована: Янв. 10, 2019

By employing cheap and biodegradable natural deep eutectic solvent as the catalyst reaction media, selective selenocyanation of activated alkynes via an intermolecular H-bonding activation pathway has been achieved, which allows for efficient construction various Z-vinyl selenolates.

Язык: Английский

Процитировано

121

Photoredox-Catalyzed Sulfonylation ofO-Acyl Oximes via Iminyl Radicals with the Insertion of Sulfur Dioxide DOI
Jun Zhang, Xiaofang Li,

Wenlin Xie

и другие.

Organic Letters, Год журнала: 2019, Номер 21(13), С. 4950 - 4954

Опубликована: Июнь 10, 2019

A multicomponent sulfonylation of O-acyl oximes via iminyl radicals with the insertion sulfur dioxide under photoredox catalysis is achieved. This reaction oximes, potassium metabisulfite, alkenes, and nucleophiles visible-light irradiation efficient, giving rise to a range sulfones in moderate good yields. broad scope presented functional group compatibility.

Язык: Английский

Процитировано

112

Photoredox-catalyzed hydrosulfonylation reaction of electron-deficient alkenes with substituted Hantzsch esters and sulfur dioxide DOI

Xuefeng Wang,

Min Yang,

Wenlin Xie

и другие.

Chemical Communications, Год журнала: 2019, Номер 55(43), С. 6010 - 6013

Опубликована: Янв. 1, 2019

A sulfonylation reaction of 4-substituted Hantzsch esters, DABCO·(SO2)2, and electron-deficient alkenes at room temperature in the presence photoredox catalysis under visible light irradiation is described. Not only (E)-chalcones but also (vinylsulfonyl)benzene 2-vinylpyridine are all suitable substrates transformation. This mild conditions shows a broad substrate scope with good functional group compatibility. plausible mechanism proposed, which that esters would be radical reservoirs catalysis. The alkyl generated situ from ester trapped by sulfur dioxide to produce an alkylsulfonyl radical, then undergo further transformation leading final outcome.

Язык: Английский

Процитировано

101

Metal-catalyzed radical-type transformation of unactivated alkyl halides with C–C bond formation under photoinduced conditions DOI
S. Ye,

Tianyi Xiang,

Xiaofang Li

и другие.

Organic Chemistry Frontiers, Год журнала: 2019, Номер 6(13), С. 2183 - 2199

Опубликована: Янв. 1, 2019

Recent advances in the metal-catalyzed radical-type transformation of unactivated alkyl halides with C–C bond formation under photoinduced conditions are summarized. Usually, a broad reaction scope is observed including tertiary, secondary, and primary halides, good functional group compatibility.

Язык: Английский

Процитировано

101

Photocatalyst-Free Regioselective C–H Thiocyanation of 4-Anilinocoumarins under Visible Light DOI
Guoqing Li,

Qiuli Yan,

X. G. Gong

и другие.

ACS Sustainable Chemistry & Engineering, Год журнала: 2019, Номер 7(16), С. 14009 - 14015

Опубликована: Авг. 2, 2019

In the present study, we describe successful development of a novel and efficient C(sp2)–H thiocyanation reaction electron-rich heteroarenes arenes with readily available ammonium thiocyanate under visible light exposure. Most importantly, proceeded smoothly without addition any photocatalyst or strong oxidant, ultimately minimizing production chemical waste. The advantages this met requirements green sustainable synthetic chemistry may be widely used in organic synthesis pharmaceutical chemistry.

Язык: Английский

Процитировано

95

Photoinduced Sulfonylation Reactions through the Insertion of Sulfur Dioxide DOI
S. Ye, Xiaofang Li,

Wenlin Xie

и другие.

European Journal of Organic Chemistry, Год журнала: 2019, Номер 2020(10), С. 1274 - 1287

Опубликована: Май 3, 2019

Recent advances in the photoinduced sulfonylation reactions through insertion of sulfur dioxide are summarized. Among approaches developed reactions, via radical process can be accomplished with assistance photoredox catalysis presence visible light or under ultraviolet irradiation, depending substrates used reactions. Under conversion completed metal‐ and additive‐free conditions. It is noteworthy that alkyl halides possessing eliminable β‐hydrogen atom effective as precursors dioxide. Two parts, according to reaction pathways, introduced: (a) photo‐initiated formation subsequent capture dioxide; (b) photo‐assisted single electron transfer (SET) after During transformation, an oxidative reductive would occur catalysis.

Язык: Английский

Процитировано

93

Synthesis of β-Sulfonyl Amides through a Multicomponent Reaction with the Insertion of Sulfur Dioxide under Visible Light Irradiation DOI
Yu Zong,

Yimin Lang,

Min Yang

и другие.

Organic Letters, Год журнала: 2019, Номер 21(6), С. 1935 - 1938

Опубликована: Март 6, 2019

A multicomponent reaction of styrenes, aryldiazonium tetrafluoroborates, sulfur dioxide, nitriles, and water in the presence a photocatalyst at room temperature is performed. This vicinal aminosulfonylation styrenes with insertion dioxide under visible light irradiation proceeds efficiently excellent chemoselectivity, giving rise to corresponding β-sulfonyl amides moderate good yields.

Язык: Английский

Процитировано

82

Clean Preparation of Quinolin-2-yl Substituted Ureas in Water DOI
Long‐Yong Xie, Sha Peng, Fang Liu

и другие.

ACS Sustainable Chemistry & Engineering, Год журнала: 2019, Номер 7(7), С. 7193 - 7199

Опубликована: Март 8, 2019

An environmentally-friendly method for the clean preparation of various quinolin-2-yl substituted ureas in water under mild and toxic reagent-, base-, organic solvent-free conditions was established. In large-scale synthesis, products could be rapidly collected via simple filtration washing with ethanol. The usage readily available raw materials, 100% atom economy, high yield, excellent regioselectivity enhanced practicability this protocol.

Язык: Английский

Процитировано

80