| 1 |
Zhang WW, Wang Q, Zhang SZ, Zheng C, You SL. (SCp)Rhodium-Catalyzed Asymmetric Satoh-Miura Reaction for Building-up Axial Chirality: Counteranion-Directed Switching of Reaction Pathways. Angew Chem Int Ed Engl 2023;62:e202214460. [PMID: 36383091 DOI: 10.1002/anie.202214460] [Reference Citation Analysis]
|
| 2 |
Binnani C, Singh SK. Arene–Ruthenium(II) Complexes in CH Functionalization: Role of Ligands. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0039] [Reference Citation Analysis]
|
| 3 |
Li Y, Liou YC, Oliveira JCA, Ackermann L. Ruthenium(II)/Imidazolidine Carboxylic Acid-Catalyzed C-H Alkylation for Central and Axial Double Enantio-Induction. Angew Chem Int Ed Engl 2022;61:e202212595. [PMID: 36108175 DOI: 10.1002/anie.202212595] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
|
| 4 |
Chatani N. Rhodium‐Catalyzed C(sp 3 )H Functionalization. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0020] [Reference Citation Analysis]
|
| 5 |
Chen J, Teng M, Huang F, Song H, Wang Z, Zhuang H, Wu Y, Wu X, Yao Q, Shi B. Cobalt/Salox‐Catalyzed Enantioselective Dehydrogenative C−H Alkoxylation and Amination. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202210106] [Reference Citation Analysis]
|
| 6 |
Yue Q, Liu B, Liao G, Shi B. Binaphthyl Scaffold: A Class of Versatile Structure in Asymmetric C–H Functionalization. ACS Catal . [DOI: 10.1021/acscatal.2c02193] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 7 |
Li J, Xie P, Zhou T, Qian P, Zhou Y, Li H, Hong X, Shi B. Ir(III)-Catalyzed Asymmetric C–H Activation/Annulation of Sulfoximines Assisted by the Hydrogen-Bonding Interaction. ACS Catal . [DOI: 10.1021/acscatal.2c00962] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 8 |
Hirata Y, Sekine D, Kato Y, Lin L, Kojima M, Yoshino T, Matsunaga S. Cobalt(III)/Chiral Carboxylic Acid-Catalyzed Enantioselective Synthesis of Benzothiadiazine-1-oxides via C-H Activation. Angew Chem Int Ed Engl 2022;61:e202205341. [PMID: 35491238 DOI: 10.1002/anie.202205341] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 9 |
Vidal X, Font M, Gulías M, Mascareñas JL. Transition Metal‐Catalyzed Desymmetrizations Based on CH Activation Processes. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0138] [Reference Citation Analysis]
|
| 10 |
Hirata Y, Sekine D, Kato Y, Lin L, Kojima M, Yoshino T, Matsunaga S. Cobalt(III)/Chiral Carboxylic Acid‐Catalyzed Enantioselective Synthesis of Benzothiadiazine‐1‐oxides via C−H Activation. Angewandte Chemie. [DOI: 10.1002/ange.202205341] [Reference Citation Analysis]
|
| 11 |
Dethe DH, Beeralingappa NC, Siddiqui SA, Chavan PN. Asymmetric Ru/Cinchonine Dual Catalysis for the One-Pot Synthesis of Optically Active Phthalides from Benzoic Acids and Acrylates. J Org Chem 2022. [PMID: 35266689 DOI: 10.1021/acs.joc.1c02961] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
|
| 12 |
Li HL, Yang DF, Jing HQ, Antilla JC, Kuninobu Y. Palladium-Catalyzed Enantioselective C(sp3)-H Arylation of 2-Propyl Azaaryls Enabled by an Amino Acid Ligand. Org Lett 2022. [PMID: 35142219 DOI: 10.1021/acs.orglett.1c04215] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
|
| 13 |
Yu X, Zhang Z, Niu J, Shi B. Coordination-assisted, transition-metal-catalyzed enantioselective desymmetric C–H functionalization. Org Chem Front . [DOI: 10.1039/d1qo01884a] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 11.0] [Reference Citation Analysis]
|
| 14 |
Shi Y, Bai W, Mu W, Li J, Yu J, Lian B. Research Progress on Density Functional Theory Study of Palladium-Catalyzed C—H Functionalization to Form C—X (X=O, N, F, I, …) Bonds. Chinese Journal of Organic Chemistry 2022;42:1346. [DOI: 10.6023/cjoc202110027] [Reference Citation Analysis]
|
| 15 |
Zhang C, Hu X, Dai Y, Yin P, Wang C, Duan W. Asymmetric C–H Activation for the Synthesis of P- and Axially Chiral Biaryl Phosphine Oxides by an Achiral Cp*Ir Catalyst with Chiral Carboxylic Amide. ACS Catal 2022;12:193-9. [DOI: 10.1021/acscatal.1c05080] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
|
| 16 |
Hirose J, Wakikawa T, Satake S, Kojima M, Hatano M, Ishihara K, Yoshino T, Matsunaga S. Cp*Rh III /Chiral Disulfonate/CuOAc Catalyst System for the Enantioselective Intramolecular Oxyamination of Alkenes. ACS Catal 2021;11:15187-93. [DOI: 10.1021/acscatal.1c04699] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
|
| 17 |
Zhang Q, Wu L, Shi B. Forging C−heteroatom bonds by transition metal-catalyzed enantioselective C–H functionalization. Chem 2021. [DOI: 10.1016/j.chempr.2021.11.015] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 10.5] [Reference Citation Analysis]
|
| 18 |
Yang C, Li F, Wu TR, Cui R, Wu BB, Jin RX, Li Y, Wang XS. Development of Axially Chiral Styrene-Type Carboxylic Acid Ligands via Palladium-Catalyzed Asymmetric C-H Alkynylation. Org Lett 2021;23:8132-7. [PMID: 34647750 DOI: 10.1021/acs.orglett.1c02692] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
|
| 19 |
Yuan WK, Shi BF. Synthesis of Chiral Spirolactams via Sequential C-H Olefination/Asymmetric [4+1] Spirocyclization under a Simple CoII /Chiral Spiro Phosphoric Acid Binary System. Angew Chem Int Ed Engl 2021;60:23187-92. [PMID: 34435722 DOI: 10.1002/anie.202108853] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 9.0] [Reference Citation Analysis]
|
| 20 |
Ruijie S, Guomin S, Yanxin L, Ning W, Chencheng F, Xu J, Yanhui L, Chengzhi G, Yaqing F, Shuxian M. Unique PDT and PTT synergistic effect between TPE and BODIPY. Chem Commun (Camb) 2021;57:10035-8. [PMID: 34505599 DOI: 10.1039/d1cc04481h] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
|
| 21 |
Yuan W, Shi B. Synthesis of Chiral Spirolactams via Sequential C−H Olefination/Asymmetric [4+1] Spirocyclization under a Simple Co II /Chiral Spiro Phosphoric Acid Binary System. Angewandte Chemie 2021;133:23371-6. [DOI: 10.1002/ange.202108853] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
|
| 22 |
Pan C, Yin SY, Gu Q, You SL. CpxM(iii)-catalyzed enantioselective C-H functionalization through migratory insertion of metal-carbenes/nitrenes. Org Biomol Chem 2021;19:7264-75. [PMID: 34612356 DOI: 10.1039/d1ob01248g] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 4.5] [Reference Citation Analysis]
|
| 23 |
Yoshino T, Matsunaga S. Chiral Carboxylic Acid Assisted Enantioselective C–H Activation with Achiral Cp x M III (M = Co, Rh, Ir) Catalysts. ACS Catal 2021;11:6455-66. [DOI: 10.1021/acscatal.1c01351] [Cited by in Crossref: 45] [Cited by in F6Publishing: 52] [Article Influence: 22.5] [Reference Citation Analysis]
|
| 24 |
Zhou T, Qian PF, Li JY, Zhou YB, Li HC, Chen HY, Shi BF. Efficient Synthesis of Sulfur-Stereogenic Sulfoximines via Ru(II)-Catalyzed Enantioselective C-H Functionalization Enabled by Chiral Carboxylic Acid. J Am Chem Soc 2021;143:6810-6. [PMID: 33909436 DOI: 10.1021/jacs.1c03111] [Cited by in Crossref: 44] [Cited by in F6Publishing: 53] [Article Influence: 22.0] [Reference Citation Analysis]
|
| 25 |
Mou Q, Zhao R, Niu R, Fukagawa S, Shigeno T, Yoshino T, Matsunaga S, Sun B. Cp*Ir( iii )/chiral carboxylic acid-catalyzed enantioselective C–H alkylation of ferrocene carboxamides with diazomalonates. Org Chem Front 2021;8:6923-30. [DOI: 10.1039/d1qo01344k] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
|
