Meet our Associate Editor in Organic Chemistry: Yong-Qiang Tu
Professor Yong-Qiang Tu (Lanzhou University, China) handles submissions to Chemical Communications (ChemComm) in organic chemistry.
Yong-Qiang’s research interests centre on tandem rearrangement reactions and their application to the total syntheses of bioactive alkaloids, synthetic studies of biologically active natural products, and the construction of C-C and C-N bonds via C-H functionalisations. We invite you to submit your urgent research to his editorial office.
Read Yong-Qiang’s Editor’s Choice selection of ChemComm articles by clicking on the links below – all articles are FREE for a limited period!
ChemComm is the home of urgent high quality communications from across the chemical sciences. With a world-renowned reputation for quality and fast times to publication (average of 40 days), ChemComm is the ideal place to publish your research.
Yong-Qiang Tu’s Editor’s Choice:
Enantioselective total synthesis of (+)-brazilin, (−)-brazilein and (+)-brazilide A
Xuequan Wang, Hongbin Zhang, Xiaodong Yang, Jingfeng Zhao and Chengxue Pan
DOI: 10.1039/C3CC42385A
Domino Rh-catalyzed hydroformylation–double cyclization of o-amino cinnamyl derivatives: applications to the formal total syntheses of physostigmine and physovenine
Wen-Hua Chiou, Chien-Lun Kao, Jui-Chi Tsai and Yun-Man Chang
DOI: 10.1039/C3CC43257B
An organocatalytic asymmetric sequential allylic alkylation–cyclization of Morita–Baylis–Hillman carbonates and 3-hydroxyoxindoles
Qi-Lin Wang, Lin Peng, Fei-Ying Wang, Ming-Liang Zhang, Li-Na Jia, Fang Tian, Xiao-Ying Xu and Li-Xin Wang
DOI: 10.1039/C3CC45139A
A modular total synthesis of (±)-trigonoliimine C
B. Narendraprasad Reddy and Chepuri V. Ramana
DOI: 10.1039/C3CC45512B
Synthetic modification of salinomycin: selective O-acylation and biological evaluation
Björn Borgström, Xiaoli Huang, Martin Pošta, Cecilia Hegardt, Stina Oredsson and Daniel Strand
DOI: 10.1039/C3CC45983G
Highly enantioselective synthesis of chiral 7-ring O- and N-heterocycles by a one-pot nitro-Michael–cyclization tandem reaction
Renate Rohlmann, Constantin-Gabriel Daniliuc and Olga García Mancheño
DOI: 10.1039/C3CC47397J
A new versatile approach to synthesise enantioenriched 3-hydroxyoxindoles, 1,3-dihydroisobenzofuran and 3-isochromanone derivatives by a rhodium-catalyzed asymmetric arylation–cyclization sequence
Yi Li, Dong-Xing Zhu and Ming-Hua Xu
DOI: 10.1039/C3CC47927G
Enantioselective total synthesis of virosaine A and bubbialidine
Hideki Miyatake-Ondozabal, Linda M. Bannwarta and Karl Gademann
DOI: 10.1039/C3CC38783F
A catalytic multicomponent coupling reaction for the enantioselective synthesis of spiroacetals
Lara Cala, Abraham Mendoza, Francisco J. Fañanás and Félix Rodríguez
DOI: 10.1039/C3CC00118K
An easy access to fluoroalkanes by deoxygenative hydrofluorination of carbonyl compounds via their tosylhydrazones
Arvind K. Yadav, Vishnu P. Srivastava and Lal Dhar S. Yadav
DOI: 10.1039/C3CC00122A
You might also be interested in these ChemComm Themed Collections:
Organocatalysis
Guest edited by Keiji Maruoka, Hisashi Yamamoto, Liu-Zhu Gong and Benjamin List
Nucleic acids: new life, new materials
Guest edited by Mike Gait, Makoto Komiyama, David Liu, Jason Micklefield, Ned Seeman and Oliver Seitz
On Wednesday evening, the 2014 RSC Haworth Memorial Lecture will be delivered by 
symbol on our website.