Simple and practical one-step synthesis of new 1,3-dienic δ-sultones from terminal alkynes and some synthetic applications of these compounds; Journal of Sulfur Chemistry; Vol. 32, iss. 1
| Parent link: | Journal of Sulfur Chemistry Vol. 32, iss. 1.— 2011.— [P. 3-16] |
|---|---|
| Autres auteurs: | , , , , , |
| Résumé: | Title screen 1,3-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 Режим доступа: по договору с организацией-держателем ресурса |
| Langue: | anglais |
| Publié: |
2011
|
| Sujets: | |
| Accès en ligne: | http://dx.doi.org/10.1080/17415993.2010.537339 |
| Format: | MixedMaterials Électronique Chapitre de livre |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=636568 |
MARC
| LEADER | 00000naa0a2200000 4500 | ||
|---|---|---|---|
| 001 | 636568 | ||
| 005 | 20250331094349.0 | ||
| 035 | |a (RuTPU)RU\TPU\network\598 | ||
| 090 | |a 636568 | ||
| 100 | |a 20140217d2011 k||y0rusy50 ba | ||
| 101 | 0 | |a eng | |
| 102 | |a US | ||
| 135 | |a drnn ---uucaa | ||
| 181 | 0 | |a i | |
| 182 | 0 | |a b | |
| 200 | 1 | |a Simple and practical one-step synthesis of new 1,3-dienic δ-sultones from terminal alkynes and some synthetic applications of these compounds |f J. Gaitzsch [et al.] | |
| 203 | |a Text |c electronic | ||
| 300 | |a Title screen | ||
| 320 | |a [References: p.16 (17 tit.)] | ||
| 330 | |a 1,3-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 | |a Режим доступа: по договору с организацией-держателем ресурса | ||
| 461 | |t Journal of Sulfur Chemistry | ||
| 463 | |t Vol. 32, iss. 1 |v [P. 3-16] |d 2011 | ||
| 610 | 1 | |a электронный ресурс | |
| 610 | 1 | |a труды учёных ТПУ | |
| 610 | 1 | |a алкины | |
| 610 | 1 | |a alkynes | |
| 610 | 1 | |a bromination | |
| 610 | 1 | |a бромирование | |
| 701 | 1 | |a Gaitzsch |b J. |g Jens | |
| 701 | 1 | |a Rogachev |b V. O. |c chemist |c Engineer of Tomsk Polytechnic University, Doctor of chemical sciences |f 1975- |g Victor Olegovich |3 (RuTPU)RU\TPU\pers\31836 | |
| 701 | 1 | |a Metz |b Р. |g Peter | |
| 701 | 1 | |a Filimonov |b V. D. |c Russian chemist |c Professor of the TPU |f 1945- |g Viktor Dmitrievich |3 (RuTPU)RU\TPU\pers\26423 |9 12127 | |
| 701 | 1 | |a Zahel |b М. |g Martin | |
| 701 | 1 | |a Kataeva |b О. |g Olga | |
| 801 | 2 | |a RU |b 63413507 |c 20180306 |g RCR | |
| 856 | 4 | |u http://dx.doi.org/10.1080/17415993.2010.537339 | |
| 942 | |c CF | ||