Literature DB >> 20361745

(2-Nitrophenyl)acetyl: a new, selectively removable hydroxyl protecting group.

Katalin Daragics1, Péter Fügedi.   

Abstract

The utility of the (2-nitrophenyl)acetyl (NPAc) group for the protection of hydroxyl functions is reported. (2-Nitrophenyl)acetates are readily prepared starting from the commercially available, inexpensive (2-nitrophenyl)acetic acid, and these esters are stable under a series of common carbohydrate transformations. The NPAc group can be removed selectively using Zn and NH(4)Cl without affecting a series of common protecting groups. This new protecting group is orthogonal with the commonly used tert-butyldimethylsilyl, levulinoyl, 9-fluorenylmethoxycarbonyl, naphthylmethyl, and p-methoxybenzyl groups.

Entities:  

Year:  2010        PMID: 20361745     DOI: 10.1021/ol100562f

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

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2.  Broadening the Scope of the Reverse Orthogonal Strategy for Oligosaccharide Synthesis.

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3.  Synthetic Carbohydrate Chemistry and Translational Medicine.

Authors:  Sachin S Shivatare; Chi-Huey Wong
Journal:  J Org Chem       Date:  2020-10-30       Impact factor: 4.354

4.  Chemical Glucosylation of Labile Natural Products Using a (2-Nitrophenyl)acetyl-Protected Glucosyl Acetimidate Donor.

Authors:  Julia Weber; Markus Schwarz; Andrea Schiefer; Christian Hametner; Georg Häubl; Johannes Fröhlich; Hannes Mikula
Journal:  European J Org Chem       Date:  2018-04-26
  4 in total

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