Deacetylation of per-acetatylated glycopyranosides: an overall pattern for acidic catalyzis; Chemical Physics Letters; Vol. 723

Podrobná bibliografie
Parent link:Chemical Physics Letters
Vol. 723.— 2019.— [P. 123-127]
Korporace: Национальный исследовательский Томский политехнический университет Инженерная школа новых производственных технологий Научно-образовательный центр Н. М. Кижнера, Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Další autoři: Nasibullin R. T. Rinat Talgatovich, Valiev R. R. Rashid Rinatovich, Fayskanova K. M. Kseniya Mikhaylovna, Stepanova E. V. Elena Vladimirovna, Cherepanov V. N. Viktor Nikolaevich, Filimonov V. D. Viktor Dmitrievich, Sundholm D. Dage
Shrnutí:Title screen
Acetyl protecting groups are commonly used in carbohydrate chemistry. Partially acetylated arylglycosides arenot only useful building blocks in syntheses, but they are also substantial for plant metabolism. Nonselectivebase catalysis is often used for removing the acetyl groups. Even though acid-catalyzed deacetylation might bemore selective, it is seldom used in carbohydrate chemistry, because it has not been thoroughly investigated. Inthis work, we study the acid-catalyzed deacetylation ofper-acetylated phenyl glycosides experimentally andcomputationally by using density functional theory (DFT) calculations. Based on quantum modeling, we design ageneral scheme for the stepwise acid-catalyzed deacetylation of arylglycosidesper-acetates. The approach canalso be applied on gluco- and galactopyranosides. We have studied the deacetylation reaction in solvents ofdifferent polarity and found that the activation barriers of the stepwise deacetylation mechanism increase withincreasing polarity of the solvent.
Режим доступа: по договору с организацией-держателем ресурса
Jazyk:angličtina
Vydáno: 2019
Témata:
On-line přístup:https://doi.org/10.1016/j.cplett.2019.03.022
Médium: Elektronický zdroj Kapitola
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=664288

MARC

LEADER 00000naa0a2200000 4500
001 664288
005 20250424141843.0
035 |a (RuTPU)RU\TPU\network\35472 
035 |a RU\TPU\network\24413 
090 |a 664288 
100 |a 20210406d2019 k||y0rusy50 ba 
101 0 |a eng 
102 |a NL 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Deacetylation of per-acetatylated glycopyranosides: an overall pattern for acidic catalyzis  |f R. T. Nasibullin, R. R. Valiev, K. M. Fayskanova [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 39 tit.] 
330 |a Acetyl protecting groups are commonly used in carbohydrate chemistry. Partially acetylated arylglycosides arenot only useful building blocks in syntheses, but they are also substantial for plant metabolism. Nonselectivebase catalysis is often used for removing the acetyl groups. Even though acid-catalyzed deacetylation might bemore selective, it is seldom used in carbohydrate chemistry, because it has not been thoroughly investigated. Inthis work, we study the acid-catalyzed deacetylation ofper-acetylated phenyl glycosides experimentally andcomputationally by using density functional theory (DFT) calculations. Based on quantum modeling, we design ageneral scheme for the stepwise acid-catalyzed deacetylation of arylglycosidesper-acetates. The approach canalso be applied on gluco- and galactopyranosides. We have studied the deacetylation reaction in solvents ofdifferent polarity and found that the activation barriers of the stepwise deacetylation mechanism increase withincreasing polarity of the solvent. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
338 |b Российский фонд фундаментальных исследований  |d 18-33-00365\18 мол_а 
461 |t Chemical Physics Letters 
463 |t Vol. 723  |v [P. 123-127]  |d 2019 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a aryl glycosides 
610 1 |a acid-catalyzed deacetylation 
610 1 |a transition state modelling 
610 1 |a activation energy calculation 
610 1 |a моделирование 
610 1 |a переходные состояния 
610 1 |a энергия активации 
610 1 |a кислотный катализ 
701 1 |a Nasibullin  |b R. T.  |g Rinat Talgatovich 
701 1 |a Valiev  |b R. R.  |c chemist  |c Assistant of Tomsk Polytechnic University  |f 1983-  |g Rashid Rinatovich  |3 (RuTPU)RU\TPU\pers\34114 
701 1 |a Fayskanova  |b K. M.  |g Kseniya Mikhaylovna 
701 1 |a Stepanova  |b E. V.  |c chemist  |c engineer of Tomsk Polytechnic University  |f 1978-  |g Elena Vladimirovna  |3 (RuTPU)RU\TPU\pers\34245 
701 1 |a Cherepanov  |b V. N.  |g Viktor Nikolaevich 
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 Sundholm  |b D.  |g Dage 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Инженерная школа новых производственных технологий  |b Научно-образовательный центр Н. М. Кижнера  |3 (RuTPU)RU\TPU\col\23556 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)  |c (2017- )  |3 (RuTPU)RU\TPU\col\23537 
801 0 |a RU  |b 63413507  |c 20210406  |g RCR 
850 |a 63413507 
856 4 |u https://doi.org/10.1016/j.cplett.2019.03.022 
942 |c CF