Selective hydrogenolysis of the benzyl protecting group for hydroxy function with raney nickel in the presence of the MPM (4-methoxybenzyl) and DMPM (3,4-dimethoxybenzyl) protecting groups-Reference-Cited by-同舟云学术

Selective hydrogenolysis of the benzyl protecting group for hydroxy function with raney nickel in the presence of the MPM (4-methoxybenzyl) and DMPM (3,4-dimethoxybenzyl) protecting groups

Published:1984-01 Issue:47 Volume:25 Page:5397-5400
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Oikawa Yuji,Tanaka Tatsuyoshi,Horita Kiyoshi,Yonemitsu Osamu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Specific removal of o-methoxybenzyl protection by DDQ oxidation.

2. Kinetic acetalization for 1,2- and 1,3-diol protection by the reaction of p-methoxyphenylmethyl methyl ether with DDQ

3. Protection of hydroxy groups by intramolecular oxidative formation of methoxybenzylidene acetals with DDQ

4. Y. Oikawa, T. Tanaka, K. Horita, T. Yoshioka, and O. Yonemitsu, Tetrahedron Lett., submitted.

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