H. Dao S. A. B. / Creative Commons / DFT / Sustainable Chemical Technologies / /
Country
United Kingdom / / /
Event
Business Partnership / Environmental Issue / /
Facility
University of Bath / /
IndustryTerm
by-product / activation energy barriers / energy intensive process / metal free cyclisation / insertion products / Online RSC Advances Table / viscous solution / Online Open Access Article / mono-insertion products / Online Communication RSC Advances On-going work / /
Organization
American Chemical Society / University of Bath / Centre for Sustainable Chemical Technologies / Royal Society of Chemistry / University of Bath Online Publication Store / UK Engineering and Physical Sciences Research Council / Department of Chemistry / /
Person
M. Fujiwara / Georgina L. Gregory / A. Mirchandani / Marion Ulmann / D. J. Darensbourg / P. G. Jessop / Sue Whorrod / L. Luco / X. Li / J. L. Hedrick / A. R. Smith / A. Zwoster / D. P. Sanders / D. J. Coady / K. Fukushima / F. Zheng / C. A. Eckert / Antoine Buchard / A. Nelson / Roger Whorrod / C. L. Liotta / I. Kutnyakov / Adv / H. Sardon / D. J. Heldebrant / M. Yasumoto / A. Kohl / O. G. Nik / / /
Gregory, G. L., Ulmann, M. and Buchard, ASynthesis of 6-membered cyclic carbonates from 1,3-diols and low CO2 pressure: a novel mild strategy to replace phosgene reagents. RSC Advances, pp.