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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
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry

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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