| dc.contributor.author | Tverdokhleb, N. M. | |
| dc.contributor.author | Khoroshilov, G. E. | |
| dc.contributor.author | Dotsenko, V. V. | |
| dc.contributor.author | Твердохлеб, Н. М. | |
| dc.contributor.author | Хорошилов, Г. Е. | |
| dc.contributor.author | Дотсенко, В. В. | |
| dc.date.accessioned | 2018-06-23T21:20:48Z | |
| dc.date.available | 2018-06-23T21:20:48Z | |
| dc.date.issued | 2014 | |
| dc.identifier.uri | http://hdl.handle.net/123456789/2772 | |
| dc.description | Tverdokhleba N. M. Cascade synthesis of pyrido[3,2-a]indolizines by reaction of Kröhnke–Mukaiyama salts with malononitrile dimer / N. M.Tverdokhleba, G. E.Khoroshilova, V. V.Dotsenko // Tetrahedron Letters. - 2014. - Vol. 55 (26 November). - P. 6593-6595. | uk_UA |
| dc.description.abstract | An efficient protocol for the synthesis of highly functionalized 2-aminoindolizines and pyrido[3,2-a]indolizines has been achieved via the reaction of N-RC(O)CH2-2-chloropyridinium bromides with 2-amino-1,1,3-tricyanopropene in the presence of Et3N. The reaction of N-allyl-2-chloropyridinium bromide with 2-amino-1,1,3-tricyanopropene in the presence of Et3N gives 3-[1-allylpyridin-2(1Н)-ylidene]-2-aminoprop-1-ene-1,1,3-tricarbonitrile, which could be cyclized to give [2-amino-(2-amino-3-vinylindolizin-1-yl)methylene]malononitrile upon treatment with KOH–DMF. | uk_UA |
| dc.language.iso | other | uk_UA |
| dc.subject | хімічні науки | uk_UA |
| dc.title | Cascade synthesis of pyrido[3,2-a]indolizines by reaction of Kröhnke–Mukaiyama salts with malononitrile dimer | uk_UA |
| dc.type | Article | uk_UA |