Carbene‐Catalyzed and Pnictogen Bond‐Assisted Access to PIII‐Stereogenic Compounds DOI
Jianjian Liu, Rui Deng, Xuyang Liang

и другие.

Angewandte Chemie, Год журнала: 2024, Номер 136(28)

Опубликована: Апрель 26, 2024

Abstract Intermolecular pnictogen bonding (PnB) catalysis has received increased interest in non‐covalent organocatalysis. It been demonstrated that organic electron‐deficient atoms can act as prospective Lewis acids. Here, we present a catalytic approach for the asymmetric synthesis of chiral P III compounds by combining intramolecular PnB interactions and carbene catalysis. Our design features pre‐chiral phosphorus molecule bearing two electron‐withdrawing benzoyl groups, resulting formation σ‐hole at atom. X‐ray interaction (NCI) analysis indicate model substrates exhibit intrinsic between oxygen atom formyl group This induces conformational locking effect, leading to crystallization substrate preferred conformation ( 2 1 group). Under N –heterocyclic carbene, aldehyde moiety activated bond selectively reacts with an alcohol yield corresponding monoester/phosphorus product excellent enantioselectivity. acidic center, aroused non‐polarized interaction, assists selective regulations, providing unique opportunities beyond.

Язык: Английский

Carbene‐Catalyzed and Pnictogen Bond‐Assisted Access to PIII‐Stereogenic Compounds DOI
Jianjian Liu, Rui Deng, Xuyang Liang

и другие.

Angewandte Chemie International Edition, Год журнала: 2024, Номер 63(28)

Опубликована: Апрель 26, 2024

Intermolecular pnictogen bonding (PnB) catalysis has received increased interest in non-covalent organocatalysis. It been demonstrated that organic electron-deficient atoms can act as prospective Lewis acids. Here, we present a catalytic approach for the asymmetric synthesis of chiral P

Язык: Английский

Процитировано

8

Cobalt-catalyzed enantioselective hydroetherification of alkenes and symmetric 1,3-diketones DOI

Meihui Guan,

Lihan Zhu, Yue Wang

и другие.

Chem Catalysis, Год журнала: 2024, Номер unknown, С. 101126 - 101126

Опубликована: Окт. 1, 2024

Язык: Английский

Процитировано

3

Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-nosylimines DOI Open Access
Xiaolin Wang, Haibin Jiang, Sheng‐Cai Zheng

и другие.

Опубликована: Янв. 25, 2024

A enantioselective tandem transformation concerning asymmetric allylic decarboxylative addition and cyclization of N-nosylimines with vinylethylene carbonates (VECs) in the presence [Rh(C2H4)2Cl]2, chiral sulfoxide-N-olefin tridentate ligand has been developed. The reaction VECs various substituted proceeded smoothly under mild conditions, giving highly functionalized oxazolidine frameworks good to high yields excellent enantioselectivity.

Язык: Английский

Процитировано

1

Rhodium-Catalyzed Tandem Asymmetric Allylic Decarboxylative Addition and Cyclization of Vinylethylene Carbonates with N-Nosylimines DOI Creative Commons
Xiaolin Wang, Haibin Jiang, Sheng‐Cai Zheng

и другие.

Molecules, Год журнала: 2024, Номер 29(5), С. 1019 - 1019

Опубликована: Фев. 26, 2024

A enantioselective tandem transformation, concerning asymmetric allylic decarboxylative addition and cyclization of

Язык: Английский

Процитировано

1

COAP/Pd-catalyzed asymmetric linear allylic alkylation for synthesizing chiral 3,3′-disubstituted oxindoles bearing all-carbon quaternary stereocenters and primary allylic alcohol structures DOI
Wenkai Liu, Bailin Wang,

Xing‐Yun Sun

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(18), С. 5196 - 5201

Опубликована: Янв. 1, 2024

A linear asymmetric allylic alkylation of vinyloxirane catalyzed by a chiral oxalamide–phosphine (COAP)/Pd(0) complex was reported. Various 3,3′-oxindole derivatives were achieved in good yields with excellent regio- and enantioselectivity.

Язык: Английский

Процитировано

1

Cobalt-Catalyzed Enantioselective Reductive Addition of Ketimine with Cyclopropyl Chloride to Construct the Chiral Amino Esters Bearing Cyclopropyl Fragments DOI
Jiangtao Hu, Tingting Xia, Xianqing Wu

и другие.

Organic Chemistry Frontiers, Год журнала: 2024, Номер 11(22), С. 6311 - 6318

Опубликована: Янв. 1, 2024

Co-catalyzed asymmetric reductive addition of ketimine with cyclopropyl chloride has been realized to access diverse chiral amino esters bearing fragments broad functional group tolerance and excellent enantioselectivities.

Язык: Английский

Процитировано

1

Carbene‐Catalyzed and Pnictogen Bond‐Assisted Access to PIII‐Stereogenic Compounds DOI
Jianjian Liu, Rui Deng, Xuyang Liang

и другие.

Angewandte Chemie, Год журнала: 2024, Номер 136(28)

Опубликована: Апрель 26, 2024

Abstract Intermolecular pnictogen bonding (PnB) catalysis has received increased interest in non‐covalent organocatalysis. It been demonstrated that organic electron‐deficient atoms can act as prospective Lewis acids. Here, we present a catalytic approach for the asymmetric synthesis of chiral P III compounds by combining intramolecular PnB interactions and carbene catalysis. Our design features pre‐chiral phosphorus molecule bearing two electron‐withdrawing benzoyl groups, resulting formation σ‐hole at atom. X‐ray interaction (NCI) analysis indicate model substrates exhibit intrinsic between oxygen atom formyl group This induces conformational locking effect, leading to crystallization substrate preferred conformation ( 2 1 group). Under N –heterocyclic carbene, aldehyde moiety activated bond selectively reacts with an alcohol yield corresponding monoester/phosphorus product excellent enantioselectivity. acidic center, aroused non‐polarized interaction, assists selective regulations, providing unique opportunities beyond.

Язык: Английский

Процитировано

0