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Chin. J. Org. Chem. ›› 2010, Vol. 30 ›› Issue (02): 276-281. Previous Articles Next Articles
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朱晓鹤,倪成良,宋秀庆,闫红*,钟儒刚
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基金资助:
北京市自然科学基金(No. 200710005002)资助项目;国家自然科学基金(No. 20872009)资助项目;国家级.国家自然科学基金
Zhu Xiaohe Ni Chengliang Song Xiuqing Yan Hong* Zhong Rugang
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3,9-Diazahexacyclo[6.4.0.02,7.04,11.05,10]dodecanes were synthesized by a head-to-tail [2+2] photocycloaddition of 1,4-dihydropyridines. Various factors such as solvents, the concentrations of 1,4-dihydropyridine, wavelength of UV and reaction time, were studied in details. An efficient method of synthesizing 3,9-diazatetraasteranes was found, and 12 compounds were ob-tained and characterized by IR, 1H NMR, 13C NMR, MS and HRMS tech-niques.
Key words: 3,9-diazatetraasterane, 1,4-dihydropyridine, [2+2] photocycloaddition
SHU Xiao-He, NI Cheng-Liang, SONG Xiu-Qiang, YAN Gong, ZHONG Ru-Gang. Synthesis of 3,9-Diazatetraasteranes[J]. Chin. J. Org. Chem., 2010, 30(02): 276-281.
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