Acid catalyzed intramolecular attack of β-phenylthioureido group on amide function. Parallel formation of thiodihydrouracil and 4-iminothiodihydrouracil. Different pathways in the Edman degradation reaction in the formation of six- versus five-membered cy-Reference-Cited by-同舟云学术

Acid catalyzed intramolecular attack of β-phenylthioureido group on amide function. Parallel formation of thiodihydrouracil and 4-iminothiodihydrouracil. Different pathways in the Edman degradation reaction in the formation of six- versus five-membered cy

Published:2007-12-04 Issue:1 Volume:21 Page:14-22
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Pojarlieff Ivan G.,Blagoeva Iva B.,Toteva Maria M.,Atay Ergun,Angelova Violina T.,Vassilev Nikolay G.,Koedjikov Asen H.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.1269/fullpdf

Reference18 articles.

1. Method for Determination of the Amino Acid Sequence in Peptides.

2. On the Mechanism of the Phenyl Isothiocyanate Degradation of Peptides.

3. Reactions of Allyl Isothiocyanate with Alanine, Glycine, and Several Peptides in Model Systems

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