Problems associated with use of the benzyloxymethyl protecting group for histidines Formaldehyde adducts formed during cleavage by hydrogen fluoride 1-Reference-Cited by-同舟云学术

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Problems associated with use of the benzyloxymethyl protecting group for histidines Formaldehyde adducts formed during cleavage by hydrogen fluoride 1

Published:2009-01-12 Issue:4 Volume:36 Page:350-355
ISSN:0367-8377
Container-title:International Journal of Peptide and Protein Research
language:en
Short-container-title:

Author:

MITCHELL MARK A.,RUNGE THOMAS A.,MATHEWS W. RODNEY,ICHHPURANI AVNEET K.,HARN NANCY K.,DOBROWOLSKI PAUL J.,ECKENRODE FRANCES M.

Publisher

Wiley

Subject

Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1990.tb01293.x/fullpdf

Reference14 articles.

1. Characterization of impurities in a synthetic renin substrate peptide by fast-atom bombardment mass spectrometry and hybrid tandem mass spectrometry

2. Brown , T. Jones , J.H. 1981 J. C. S. Chem. Commun. 648 649

3. Further studies on the protection of histidine side chains in peptide synthesis: the use of the π-benzyloxymethyl group

4. Tissue sulfhydryl groups

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