| 000 | 02008nam1a2200421 4500 | ||
|---|---|---|---|
| 001 | 636568 | ||
| 005 | 20231030040138.0 | ||
| 035 | _a(RuTPU)RU\TPU\network\598 | ||
| 090 | _a636568 | ||
| 100 | _a20140217a2011 k y0engy50 ba | ||
| 101 | 0 | _aeng | |
| 102 | _aUS | ||
| 135 | _adrnn ---uucaa | ||
| 181 | 0 | _ai | |
| 182 | 0 | _ab | |
| 200 | 1 |
_aSimple and practical one-step synthesis of new 1,3-dienic δ-sultones from terminal alkynes and some synthetic applications of these compounds _fJ. Gaitzsch [et al.] |
|
| 203 |
_aText _celectronic |
||
| 300 | _aTitle screen | ||
| 320 | _a[References: p.16 (17 tit.)] | ||
| 330 | _a1,3-Dienic δ -sultones 4,6-diaryl-[1,2]oxathiine 2,2-dioxides were synthesized via a one-step reaction of arylalkynes with dioxane sulfotrioxide. The reactivity of various alkynes in this reaction was investigated. The resulting sultones were brominated with Br2 or N-bromosuccinimide regioselectively α to sulfur and subsequently coupled with phenylacetylene using Sonogashira conditions | ||
| 333 | _aРежим доступа: по договору с организацией-держателем ресурса | ||
| 461 | _tJournal of Sulfur Chemistry | ||
| 463 |
_tVol. 32, iss. 1 _v[P. 3-16] _d2011 |
||
| 610 | 1 | _aэлектронный ресурс | |
| 610 | 1 | _aтруды учёных ТПУ | |
| 610 | 1 | _aалкины | |
| 610 | 1 | _aalkynes | |
| 610 | 1 | _abromination | |
| 610 | 1 | _aбромирование | |
| 701 | 1 |
_aGaitzsch _bJ. _gJens |
|
| 701 | 1 |
_aRogachev _bV. O. _cchemist _cEngineer of Tomsk Polytechnic University, Doctor of chemical sciences _f1975- _gVictor Olegovich _2stltpush _3(RuTPU)RU\TPU\pers\31836 |
|
| 701 | 1 |
_aMetz _bР. _gPeter |
|
| 701 | 1 |
_aFilimonov _bV. D. _cRussian chemist _cProfessor of the TPU _f1945- _gViktor Dmitrievich _2stltpush _3(RuTPU)RU\TPU\pers\26423 |
|
| 701 | 1 |
_aZahel _bМ. _gMartin |
|
| 701 | 1 |
_aKataeva _bО. _gOlga |
|
| 801 | 2 |
_aRU _b63413507 _c20180306 _gRCR |
|
| 856 | 4 | _uhttp://dx.doi.org/10.1080/17415993.2010.537339 | |
| 942 | _cBK | ||