ChemInform Abstract: Spirolactones of Tyrosine: Synthesis and Reaction with Nucleophiles

التفاصيل البيبلوغرافية
العنوان: ChemInform Abstract: Spirolactones of Tyrosine: Synthesis and Reaction with Nucleophiles
المؤلفون: A. Ziogas, Medhat El-Mobayed, Anton Rieker, Antun Hutinec
المصدر: ChemInform. 29
بيانات النشر: Wiley, 2010.
سنة النشر: 2010
مصطلحات موضوعية: chemistry.chemical_classification, chemistry.chemical_compound, Dipeptide, chemistry, Nucleophile, Stereochemistry, Side chain, Moiety, General Medicine, Phenols, Tyrosine synthesis, Tyrosine, Amino acid
الوصف: Several quinonoidal spirolactones (1-oxaspiro[4,5]deca-6,9-diene-2,8-diones) 12 have been synthesized chemically or electrochemically by oxidation of the corresponding tyrosine phenols 3. The spirolactones are of considerable value in peptide chemistry, because they react as active esters with amino acid esters to give dipeptides. In the latter, the side chain of the tyrosine moiety is present as a quinol (4-hydroxycyclohexa-2,5-dien-1-one) system, which can be reduced to the genuine tyrosyl dipeptide. Unsubstituted spirolactones also react as active esters but give dipeptides only in modest yields.
تدمد: 1522-2667
0931-7597
DOI: 10.1002/chin.199848212
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::789abe81e03a2ddd87887f3fd5dbdfd2
https://doi.org/10.1002/chin.199848212
Rights: CLOSED
رقم الانضمام: edsair.doi...........789abe81e03a2ddd87887f3fd5dbdfd2
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15222667
09317597
DOI:10.1002/chin.199848212