130874-92-9Relevant academic research and scientific papers
Synthesis of (2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenylbutane-2,3-diol
Bischop, Martina,Cmrecki, Vesna,Ophoven, Vera,Pietruszka, Joerg
, p. 2488 - 2490 (2008)
(2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenylbutane-2,3-diol proved to be an excellent auxiliary and stable protective group for boronic acids. Herein we report an improved practical procedure for its synthesis. Georg Thieme Verlag Stuttgart.
Microwave assisted synthesis of enantiomerically pure allylboronates
Cmrecki, Vesna,Eichenauer, Nils C.,Frey, Wolfgang,Pietruszka, J?rg
experimental part, p. 6550 - 6564 (2010/10/19)
Stable allylboronates with a stereogenic centre α to the boronic ester moiety represent versatile reagents for stereoselective synthesis of homoallylic alcohols. Use of microwave irradiation in desilylation and sigmatropic rearrangement reactions allows r
Synthesis of (2R, 3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol: A new C2-symmetric vicinal diol from dimethyl L-tartrate
Nakayama, Kensaku,Rainier, Jon D.
, p. 4165 - 4170 (2007/10/02)
A practical synthesis of a new C2-symmetric vicinal diol, (2R, 3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butanediol, from dimethyl L-tartrate involving five steps in overall yield of 38% is described.
