Are N-phthaloyl and O-allyl protective groups orthogonal?


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详细

Using allyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-d-glucopyranoside as a model substrate, it was shown that the degree of orthogonality of N-phthaloyl and O-allyl protective groups under the conditions of hydrazinolysis of the phthalimide group depends on the amount of atmospheric oxygen in the reaction mixture during the reaction and during the work-up procedure.

作者简介

A. Orlova

N. D. Zelinskiy Institute of Organic Chemistry, Russian Academy of Sciences

Email: kononov@ioc.ac.ru
俄罗斯联邦, 47 Leninskiy prosp., Moscow, 119991

D. Volodin

N. D. Zelinskiy Institute of Organic Chemistry, Russian Academy of Sciences

Email: kononov@ioc.ac.ru
俄罗斯联邦, 47 Leninskiy prosp., Moscow, 119991

A. Zinin

N. D. Zelinskiy Institute of Organic Chemistry, Russian Academy of Sciences

Email: kononov@ioc.ac.ru
俄罗斯联邦, 47 Leninskiy prosp., Moscow, 119991

L. Kononov

N. D. Zelinskiy Institute of Organic Chemistry, Russian Academy of Sciences; Moscow Physico-Technical Institute (National Research University)

编辑信件的主要联系方式.
Email: kononov@ioc.ac.ru
俄罗斯联邦, 47 Leninskiy prosp., Moscow, 119991; 9 Institutskiy per., Dolgoprudnyi, Moscow Region, 141701


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