FORMATION OF AMINOSUCCINYL PEPTIDES DURING ACIDOLYTIC DEPROTECTION FOLLOWED BY THEIR TRANSFORMATION TO PIPERAZINE-2,5-DIONE DERIVATIVES IN NEUTRAL MEDIA
- Author
- SCHON I; KISFALUDY L
GEDEON RICHTER LTD.,BUDAPEST 1475,HUN - Source
- INTERNATION. J. PEPT. PROT. RES.; DNK; DA. 1979; VOL. 14; NO 5; PP. 485-494; BIBL. 37 REF.
- Document type
- Article
- Language
- English
- Keyword (fr)
- REACTION CHIMIQUE DEPROTECTION ACIDOLYSE TRIPEPTIDE PEPTIDE CYCLIQUE DIPEPTIDE HETEROCYCLE AZOTE CYCLE 6 CHAINONS LACTAME EFFET STRUCTURE PREPARATION PIPERAZINEDIONE-2,5 DERIVE!FIN PHENYLALANINE(T-BUTOXYCARBONYLLEUCYL-T-BUTOXYASPARTYL) AMIDE!ENT PHENYLALANINE(LEUCYL-AMINOSUCCINYL) AMIDE!FIN CHIMIE ORGANIQUE
- Keyword (en)
- CHEMICAL REACTION DEPROTECTION ACIDOLYSIS TRIPEPTIDE CYCLIC PEPTIDES DIPEPTIDES NITROGEN HETEROCYCLE SIX MEMBERED RING LACTAM STRUCTURE EFFECT PREPARATION ORGANIC CHEMISTRY
- Keyword (es)
- QUIMICA ORGANICA
- Classification
- Discipline
- General chemistry and physical chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- PASCAL8060276882
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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