Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals

Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals Научная публикация

Журнал

Carbohydrate Research
ISSN: 1873-426X , E-ISSN: 0008-6215

Вых. Данные

Год: 2007, Том: 342, Номер: 3-4, Страницы: 627-630 Страниц : 4 DOI: 10.1016/j.carres.2006.10.009

Авторы

Zinin Alexander I. ¹ , Malysheva Nelly N. ¹ , Shpirt Anna M. ¹ , Torgov Vladimir I. ¹ , Kononov Leonid O. ¹

Организации

1	N. D. Zelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, Leninsky prosp., 47, 119991 Moscow, Russian Federation

Methanesulfonic acid was shown to be an efficient and convenient substitute for ethereal HCl in reductive 4,6-O-benzylidene acetal ring-opening reaction with sodium cyanoborohydride in THF. Normal regioselectivity was observed, the 6-O-benzyl ethers with free 4-OH group being the major products of the reaction.

Zinin A.I. , Malysheva N.N. , Shpirt A.M. , Torgov V.I. , Kononov L.O.
Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals
Carbohydrate Research. 2007. V.342. N3-4. P.627-630. DOI: 10.1016/j.carres.2006.10.009 WOS Scopus OpenAlex

Web of science:	WOS:000244548700027
Scopus:	2-s2.0-33846482568
OpenAlex:	W2083382471

БД	Цитирований
OpenAlex	24
Scopus	23
Web of science	20