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On the Mechanism of Condensation between 5-Amino-4, 6-dichloro- 2-methylpyrimidine and 1-Acetyl-2-imidazolin-2-one
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作者 Bin SU Hui LI +1 位作者 meng shen cai Zhong Jun LI 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第3期207-210,共4页
The condensation reaction between 5-amino-4, 6-dichloro-2-methylpyrimidine and 1-acetyl-2-imidazolin-2-one using POCl3 as solvent gave 4, 6-dichloro-2-methyl-5-(1-acetyl-tetra- hydro-imidazo-2-ylidene)-aminopyrimidine... The condensation reaction between 5-amino-4, 6-dichloro-2-methylpyrimidine and 1-acetyl-2-imidazolin-2-one using POCl3 as solvent gave 4, 6-dichloro-2-methyl-5-(1-acetyl-tetra- hydro-imidazo-2-ylidene)-aminopyrimidine predominantly and 4, 6-dichloro-2-methyl-5-{1-[1-(2- oxo-tetrahydro-imidazolyl)]-acetyene}-aminopyrimidine as by-product. No 4, 6-dichloro-2- methyl-5-(1-acetyl-2-imidazolin-2-yl)-aminopyrimidine was found. The result indicated an esterifi- cation-addition-elimination mechanism. 展开更多
关键词 MOXONIDINE X-ray single crystal diffraction GHMBC.
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STUDIES ON CARBOHYDRATES XIV.HIGHLY STEREOSELECTIVE SYNTHESIS OF 1-O-α-ACYL-D-MANNOPYRANOSE FROM THE CORRESPONDING MANNOSYL TRIMETHYLSILYL ETHER
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作者 He Qing HUANG Zhong Jun LI meng shen cai 《Chinese Chemical Letters》 SCIE CAS CSCD 1995年第4期275-278,共4页
In the presence of BF3.OEt2, 1-O-trimethylsilyi-2,3,4,6-tetra-O-benzyl-α-D-mannopyranose (1)reacted stereoselectively with a series of carboxylic acids to give the corresponding α-mannosyl carboxylates in good yield... In the presence of BF3.OEt2, 1-O-trimethylsilyi-2,3,4,6-tetra-O-benzyl-α-D-mannopyranose (1)reacted stereoselectively with a series of carboxylic acids to give the corresponding α-mannosyl carboxylates in good yields. The configuration of products was assigned mainly by 1H-NMR spectra (δH1 and 2J1.2). 展开更多
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