BUCHLOVIČ, Marian, Simona HEBANOVÁ a Milan POTÁČEK. 1,3-Dipolar cycloadditions of new 2,5-bifunctionalized 5-membered cyclic nitrones. Tetrahedron. Oxford, England: Pergamon - Elsevier Science, 2012, roč. 68, č. 14, s. 3117-3122. ISSN 0040-4020. Dostupné z: https://dx.doi.org/10.1016/j.tet.2012.01.043. |
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@article{977506, author = {Buchlovič, Marian and Hebanová, Simona and Potáček, Milan}, article_location = {Oxford, England}, article_number = {14}, doi = {http://dx.doi.org/10.1016/j.tet.2012.01.043}, keywords = {Cyclic nitrones; 1-3-Dipolar cycloadditions; Stereoselectives reactions; Dipolarophile; Nitrone complexes}, language = {eng}, issn = {0040-4020}, journal = {Tetrahedron}, title = {1,3-Dipolar cycloadditions of new 2,5-bifunctionalized 5-membered cyclic nitrones}, volume = {68}, year = {2012} }
TY - JOUR ID - 977506 AU - Buchlovič, Marian - Hebanová, Simona - Potáček, Milan PY - 2012 TI - 1,3-Dipolar cycloadditions of new 2,5-bifunctionalized 5-membered cyclic nitrones JF - Tetrahedron VL - 68 IS - 14 SP - 3117-3122 EP - 3117-3122 PB - Pergamon - Elsevier Science SN - 00404020 KW - Cyclic nitrones KW - 1-3-Dipolar cycloadditions KW - Stereoselectives reactions KW - Dipolarophile KW - Nitrone complexes N2 - A new family of 5-membered cyclic nitrones bearing functional groups at positions 2,5 were tested in 1,3-cycloadditions with various dipolarophiles. Studied reactions offered corresponding cycloaducts as single diastereomers in high yields. The reaction scope was examined, 23 compounds were isolated and fully characterized. The comparison of the reactivity was done by a study of reaction conversions while different nitrones or dipolarophiles were used. In addition, we have studied the exceptional reactivity of nitrone bearing benzylamino group in position 2. The formation of nitrone complex and evaluation of its reactivity in 1,3-DC is presented. ER -
BUCHLOVIČ, Marian, Simona HEBANOVÁ a Milan POTÁČEK. 1,3-Dipolar cycloadditions of new 2,5-bifunctionalized 5-membered cyclic nitrones. \textit{Tetrahedron}. Oxford, England: Pergamon - Elsevier Science, 2012, roč.~68, č.~14, s.~3117-3122. ISSN~0040-4020. Dostupné z: https://dx.doi.org/10.1016/j.tet.2012.01.043.
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