Literature DB >> 10814414

The use of diazabicyclo

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Abstract

[reaction: see text] In a study directed toward the use of the chloroacetyl protecting group in carbohydrate synthesis, the sterically hindered tertiary amine diazabicyclo[2.2.2]octane (DABCO) was found to give complete and selective cleavage of the chloroacetyl group in the presence of other ester functions such as benzoyl and acetyl groups at primary and/or secondary positions.

Entities:  

Year:  2000        PMID: 10814414     DOI: 10.1021/ol005567z

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


  3 in total

1.  Revealing the Pharmacophore of Ipomoeassin F through Molecular Editing.

Authors:  Guanghui Zong; Hazim Aljewari; Zhijian Hu; Wei Q Shi
Journal:  Org Lett       Date:  2016-03-21       Impact factor: 6.005

2.  Synthesis of the tumor associative α-aminooxy disaccharide of the TF antigen and its conjugation to a polysaccharide immune stimulant.

Authors:  Jean Paul Bourgault; Kevin R Trabbic; Mengchao Shi; Peter R Andreana
Journal:  Org Biomol Chem       Date:  2014-03-21       Impact factor: 3.876

3.  Design and synthesis of a novel ganglioside ligand for influenza A viruses.

Authors:  Tomohiro Nohara; Akihiro Imamura; Maho Yamaguchi; Kazuya I P J Hidari; Takashi Suzuki; Tatsuya Komori; Hiromune Ando; Hideharu Ishida; Makoto Kiso
Journal:  Molecules       Date:  2012-08-10       Impact factor: 4.411

  3 in total

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