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- Enantiodiscrimination of carboxylic acids using the diphenylprolinol NMR chiral solvating agents. Gaowei Li, Jiangming Cao, Wen Zong, Xinxiang Lei, Renxiang Tan
, Org. Chem. Front.
, 2016
, 3
, 96
- Current advances of organocatalytic Michael–Michael cascade reaction in the synthesis of highly functionalized cyclic molecules. Sabita Nayak, Pravati Panda, Sujitlal Bhakta, Sambita Kumar Mishra, Seetaram Mohapatra
, RSC Adv.
, 2016
, 6
, 96154
- An approach towards (+)-allokainic acid via diphenylprolinol-catalyzed direct cross-aldol reaction. Shashank N. Mhaldar, Santosh G. Tilve
, Org. Biomol. Chem.
, 2023
, 21
, 5469
- An efficient enantioselective approach to multifunctionalized γ-butyrolactone: concise synthesis of (+)-nephrosteranic acid. Anju Gehlawat, Ranjana Prakash, Satyendra Kumar Pandey
, RSC Adv.
, 2020
, 10
, 19655
- Symmetrical and unsymmetrical pincer complexes with group 10 metals: synthesis via aryl C–H activation and some catalytic applications. Jun-Long Niu, Xin-Qi Hao, Jun-Fang Gong, Mao-Ping Song
, Dalton Trans.
, 2011
, 40
, 5135
- Synthesis and application in asymmetric catalysis of P-stereogenic pincer–metal complexes. Yijun Xiang, Qianyi Ge, Shulei Wu, Xing Zheng, Zehua Yang
, RSC Adv.
, 2020
, 10
, 9563
- Base-promoted cascade reaction of isocyanides, selenium and amines: a practical approach to 2-aminobenzo[d][1,3]selenazines under metal-free conditions. Yi Fang, Shun-Yi Wang, Xiao-Bin Shen, Shun-Jun Ji
, Org. Chem. Front.
, 2015
, 2
, 1338
- Efficient construction of biologically important functionalized polycyclic spiro-fused carbocyclicoxindoles via an asymmetric organocatalytic quadruple-cascade reaction. Wen Ren, Xiao-Yan Wang, Jing-Jing Li, Mao Tian, Jie Liu, Liang Ouyang, Jin-Hui Wang
, RSC Adv.
, 2017
, 7
, 1863
- Enantioselective total synthesis of (S)-nakinadine B. Yuvraj Garg, Satyendra Kumar Pandey
, RSC Adv.
, 2016
, 6
, 25913
- Conjugate addition reactions of carbon nucleophiles to electron-deficient dienes. Aurelio G. Csákÿ, Gabriela de la Herrán, M. Carmen Murcia
, Chem. Soc. Rev.
, 2010
, 39
, 4080