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- Vilsmeier cyclization of α-acetyl-α-aroyl ketene-N,S-acetals: direct and efficient synthesis of halogenated pyridin-2(1H)-ones. Haifeng Yu, Yongmei Zhang, Tiechun Li, Peiqiu Liao, Quanping Diao, Guang Xin, Qingling Meng, Dongyan Hou
, RSC Adv.
, 2015
, 5
, 11293
- Transient imine as a directing group for the Pd-catalyzed anomeric C(sp3)–H arylation of 3-aminosugars. Juba Ghouilem, Sokna Bazzi, Nicolas Grimblat, Pascal Retailleau, Vincent Gandon, Samir Messaoudi
, Chem. Commun.
, 2023
, 59
, 2497
- Transient imine directing groups for the C–H functionalisation of aldehydes, ketones and amines: an update 2018–2020. Joe I. Higham, James A. Bull
, Org. Biomol. Chem.
, 2020
, 18
, 7291
- Efficient unified synthesis of diverse bridged polycyclic scaffolds using a complexity-generating ‘stitching’ annulation approach. Scott Rice, Daniel J. Cox, Stephen P. Marsden, Adam Nelson
, Chem. Commun.
, 2021
, 57
, 599
- Site-selective and diastereoselective functionalization of α-amino acid and peptide derivatives via palladium-catalyzed sp3 C–H activation. Ming Zhang, Shengliang Zhong, Yiyuan Peng, Jianwen Jiang, Yongli Zhao, Changfeng Wan, Zhenming Zhang, Rongli Zhang, Ai Qin Zhang
, Org. Chem. Front.
, 2021
, 8
, 133
- sp3 C–H activation via exo-type directing groups. Yan Xu, Guangbin Dong
, Chem. Sci.
, 2018
, 9
, 1424
- Palladium-catalyzed functionalizations of acidic and non-acidic C(sp3)–H bonds – recent advances. Gaurav Saini, Manmohan Kapur
, Chem. Commun.
, 2021
, 57
, 1693
- Diastereoselective palladium-catalyzed functionalization of prochiral C(sp3)–H bonds of aliphatic and alicyclic compounds. Srinivasarao Arulananda Babu, Yashika Aggarwal, Pooja Patel, Radha Tomar
, Chem. Commun.
, 2022
, 58
, 2612
- Aldehyde catalysis – from simple aldehydes to artificial enzymes. Zeqin Yuan, Jun Liao, Hao Jiang, Peng Cao, Yang Li
, RSC Adv.
, 2020
, 10
, 35433
- Transition metal catalyzed C–H bond activation by exo-metallacycle intermediates. Sumeet Ranjan Sahoo, Subhabrata Dutta, Shaeel A. Al-Thabaiti, Mohamed Mokhtar, Debabrata Maiti
, Chem. Commun.
, 2021
, 57
, 11885