Results 1 - 10 of 167 (Click here to explore results)

1

Understanding the role played by protic ionic liquids (PILs) and the substituent effect for enhancing the generation of Z-cinnamic acid derivatives. Rocío B. Rodríguez, Ramiro L. Zapata, María L. Salum, Rosa Erra-Balsells , Photochem. Photobiol. Sci. , 2020 , 19 , 819

A versatile access to vicinal diamine motifs by highly anti-selective asymmetric vinylogous Mannich reactions: an efficient total synthesis of (+)-absouline. Jian-Liang Ye, Hang Chen, Yu-Feng Zhang, Pei-Qiang Huang , Org. Chem. Front. , 2016 , 3 , 683

First stereoselective total synthesis of brevipolide M. Kasa Shiva Raju, Gowravaram Sabitha , Org. Biomol. Chem. , 2017 , 15 , 6393

Recent advances in the synthesis of naturally occurring pyrrolidines, pyrrolizidines and indolizidine alkaloids using proline as a unique chiral synthon. Chinmay Bhat, Santosh G. Tilve , RSC Adv. , 2014 , 4 , 5405

Design, synthesis, in vitro and in vivo evaluation of tacrine–cinnamic acid hybrids as multi-target acetyl- and butyrylcholinesterase inhibitors against Alzheimer's disease. Yao Chen, Hongzhi Lin, Jie Zhu, Kai Gu, Qi Li, Siyu He, Xin Lu, Renxiang Tan, Yuqiong Pei, Liang Wu, Yaoyao Bian, Haopeng Sun , RSC Adv. , 2017 , 7 , 33851

Stereoselective synthesis of E-3-(arylmethylidene)-5-(alkyl/aryl)-2(3H)-furanones by sequential hydroacyloxylation-Mizoroki–Heck reactions of iodoalkynes. Gopinathan Muthusamy, Sunil V. Pansare , Org. Biomol. Chem. , 2018 , 16 , 7971

An efficient palladium catalyzed Mizoroki–Heck cross-coupling in water. Sanjay N. Jadhav, Chandrashekhar V. Rode , Green Chem. , 2017 , 19 , 5958

Synthesis and biological evaluation of 2,2-dimethylbenzopyran derivatives as potent neuroprotection agents. Fangyu Du, Qifan Zhou, Xiaoxiao Fu, Yajie Shi, Yuanguang Chen, Wuhong Fang, Jingyu Yang, Guoliang Chen , RSC Adv. , 2019 , 9 , 2498

The efficient and selective catalytic oxidation of para-substituted cinnamic acid derivatives by the cytochrome P450 monooxygenase, CYP199A4. Rebecca R. Chao, James J. De Voss, Stephen G. Bell , RSC Adv. , 2016 , 6 , 55286

Mutual kinetic resolution: probing enantiorecognition phenomena and screening for kinetic resolution with racemic reagents. Stephen G. Davies, Ai M. Fletcher, Paul M. Roberts, James E. Thomson , Org. Biomol. Chem. , 2021 , 19 , 2847