Palladium-Catalyzed [3+2] Cycloaddition of 4-Vinyl-4-Butyro-lactones with Sulfamate-Derived Cyclic Imines: Construction of Sulfamate-Fused Pyrrolidines DOI
Honghao Sun,

Siyuan Ding,

Bo Wang

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

The palladium-catalyzed [3 + 2] decarboxylative cycloaddition of 4-vinyl-4-butyrolactones with sulfamate-derived cyclic imines has been developed, providing the sulfamate-fused pyrrolidine derivatives in high yields good diastereoselectivities.

Язык: Английский

4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines DOI
Yi Tang,

Rulei Zhang,

Yujie Dong

и другие.

Chemical Communications, Год журнала: 2024, Номер 60(11), С. 1436 - 1439

Опубликована: Янв. 1, 2024

Benzo-fused cyclic carbonates were designed and synthesized as a novel type of precursor π-allylpalladium zwitterionic intermediates.

Язык: Английский

Процитировано

8
Palladium-Catalyzed [5 + 4] Cycloaddition of 4-Vinyl-4-Butyrolactones with N-Tosyl Azadienes: Construction of Nine-Membered Ring DOI
Lan Wang, Sen Yang, Yi Tang

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(7), С. 5019 - 5028

Опубликована: Март 19, 2024

In this paper, we reported the palladium-catalyzed formal [5 + 4] cycloaddition reactions between 4-vinyl-4-butyrolactones (VBLs) and azadienes. Under mild reaction conditions, a wide range of benzofuran-fused 9-membered heterocyclic compounds had been provided in moderate to excellent yields with exclusive regioselectivities diastereoselectivities. The practical applicability synthesis was demonstrated through scale-up further transformation.

Язык: Английский

Процитировано

7
Cu-Catalyzed Divergent Transformations of Allenylethylene Carbonates with Diboron Reagents DOI

Si-Jie Chen,

Xiaojie Su, Yujie Dong

и другие.

Organic Letters, Год журнала: 2024, Номер 26(4), С. 960 - 965

Опубликована: Янв. 19, 2024

Divergent transformations of allenylethylene carbonates with diboron reagents catalyzed by copper are disclosed. By using CuCl/IPr·HCl as the catalyst, react B2hex2 to afford 2,4-dien-1-ols product in presence Cs2CO3 base, iPrOH additive, and 1,4-dioxane solvent. And they B2pin2 form boronic half acids NaOtBu water THF The reactions corresponding products good stereoselectivities yields, further derivatizations study mechanism also demonstrated.

Язык: Английский

Процитировано

4
Palladium-catalyzed asymmetric [4 + 3] cycloaddition of methylene-trimethylenemethane: access to seven-membered exocyclic axially chiral allenes DOI Creative Commons
Yafei Wu, Zhuo Wang,

Yuqian Shan

и другие.

Chemical Science, Год журнала: 2024, Номер 15(25), С. 9703 - 9708

Опубликована: Янв. 1, 2024

A palladium-catalyzed asymmetric [4 + 3] cycloaddition of the methylene-trimethylenemethane donor with an azadiene has been developed, affording benzofuro[3,2- b ]azepine-derived exocyclic chiral allene control axial and point chirality.

Язык: Английский

Процитировано

4
Palladium‐Catalyzed Enantioselective [4+2] Cycloaddition of 4‐Vinylbenzodioxinones with Barbiturate‐Derived Alkenes: Con‐struction of Chiral Spirobarbiturate−Chromanes DOI
Yi Tang, Mingxia Huang,

Siyuan Ding

и другие.

Chemistry - A European Journal, Год журнала: 2024, Номер 30(24)

Опубликована: Фев. 21, 2024

In this paper, Pd-catalyzed [4+2] decarboxylative cycloaddition of 4-vinylbenzodioxinones with barbiturate-derived alkenes has been developed, leading to various spirobarbiturate-chromane derivatives in high yields excellent diastereo- and enantioselectivities. The scale-up reaction further derivation the product were demonstrated. A plausible mechanism was also proposed.

Язык: Английский

Процитировано

3
Palladium-Catalyzed (4 + 1) Annulation of 4-Vinylbenzodioxinones with Sulfur Ylides: Diastereoselective Synthesis of Dihydrobenzofuran Derivatives DOI
Yi Tang, Xiaojing Sun,

Yu Tan

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(12), С. 8951 - 8959

Опубликована: Май 30, 2024

Palladium-catalyzed (4 + 1) annulation of 4-vinylbenzodioxinones with sulfur ylides has been developed to afford various dihydrobenzofuran derivatives in moderate high yields excellent diastereoselectivities. The scale-up reaction and further derivations the product worked well, demonstrating application potential current organic synthesis.

Язык: Английский

Процитировано

2
Pd-Catalyzed Sequential Intramolecular Annulation/ Intermolecular [3+2] Cycloaddition of 5-Allenyloxazolidine-2,4-diones with Dipoles: Synthesis of Spiroheterocycles DOI
Yujie Dong, Jun Liu,

Rongjin Ning

и другие.

Chemical Communications, Год журнала: 2024, Номер 60(76), С. 10516 - 10519

Опубликована: Янв. 1, 2024

Pd-catalyzed sequential intramolecular annulation/intermolecular [3+2] cycloaddition of 5-allenyloxazolidine-2,4-diones with dipoles was achieved. Under palladium catalysis, various reacted 1,3-dipoles such as nitrile

Язык: Английский

Процитировано

0
Cyclopent-4-ene-1,3-diones fused with heterocycles as promising anchor groups in non-fullerene acceptors (microreview) DOI

Sofia D. Usova,

Ekaterina A. Knyazeva, Олег А. Ракитин

и другие.

Chemistry of Heterocyclic Compounds, Год журнала: 2024, Номер 60(3-4), С. 127 - 129

Опубликована: Апрель 1, 2024

Язык: Английский

Процитировано

0
Palladium-Catalyzed [3+2] Cycloaddition of 4-Vinyl-4-Butyro-lactones with Sulfamate-Derived Cyclic Imines: Construction of Sulfamate-Fused Pyrrolidines DOI
Honghao Sun,

Siyuan Ding,

Bo Wang

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

The palladium-catalyzed [3 + 2] decarboxylative cycloaddition of 4-vinyl-4-butyrolactones with sulfamate-derived cyclic imines has been developed, providing the sulfamate-fused pyrrolidine derivatives in high yields good diastereoselectivities.

Язык: Английский

Процитировано

0