41341-99-5Relevant articles and documents
Xylonucleic acid: Synthesis, structure, and orthogonal pairing properties
Maiti, Mohitosh,Maiti, Munmun,Knies, Christine,Dumbre, Shrinivas,Lescrinier, Eveline,Rosemeyer, Helmut,Ceulemans, Arnout,Herdewijn, Piet
, p. 7189 - 7200 (2015)
There is a common interest for studying xeno-nucleic acid systems in the fields of synthetic biology and the origin of life, in particular, those with an engineered backbone and possessing novel properties. Along this line, we have investigated xylonuclei
Methanesulfonic-acid-catalysed ring opening and glycosylation of 1,2-(Acetylcyclopropane)-annulated d -lyxofuranose
Wang, Cong,Ma, Xiaofeng,Zhang, Jichao,Tang, Qin,Jiao, Wei,Shao, Huawu
, p. 4592 - 4599 (2014/08/05)
A mild and effective method for the synthesis of 2-C-branched disaccharides, glycoconjugates, and nucleoside analogues is described. 1,2-(acetylcyclopropane)-annulated D-lyxofuranose underwent ring opening catalysed by CH3SO3H to act as an efficient glycosyl donor and give the glycosylation products in good yields and with high diastereoselectivities. Copyright
InCl3 catalyzed highly diastereoselective [3 + 2] cycloaddition of 1,2-cyclopropanated sugars with aldehydes: A straightforward synthesis of persubstituted bis -tetrahydrofurans and perhydrofuro[2,3- b ]pyrans
Ma, Xiaofeng,Tang, Qin,Ke, Jun,Yang, Xinglong,Zhang, Jichao,Shao, Huawu
, p. 5170 - 5173 (2013/11/06)
A mild and efficient strategy for the construction of persubstituted bis-tetrahydrofuran and perhydrofuro[2,3-b]pyran derivatives has been developed. Persubstituted cyclization products were obtained in good to excellent yields. The [3 + 2] cycloaddition of 1,2-cyclopropanated sugars with aldehydes in the presence of InCl3 is highly diastereoselective.