Orthogonal cleavage of the 2-naphthylmethyl group in the presence of the p-methoxy phenyl-protected anomeric position and its use in carbohydrate synthesis-Reference-Cited by-同舟云学术

Orthogonal cleavage of the 2-naphthylmethyl group in the presence of the p-methoxy phenyl-protected anomeric position and its use in carbohydrate synthesis

Published:2016 Issue:6 Volume:3 Page:753-758
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Cattaneo Vittorio¹²³,Oldrini Davide¹²³,Corrado Alessio¹²³,Berti Francesco¹²³,Adamo Roberto¹²³

Affiliation:

1. GSK Vaccines

2. 53100 Siena

3. Italy

Abstract

Orthogonal removal of naphthylmethyl (NAP) and anomeric O-p-methoxyphenyl (PMP) ethers using 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and cerium(iv) ammonium nitrate, respectively, is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/QO/C6QO00144K

Reference32 articles.

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