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FORMATION OF N-ACYL DERIVATIVES OF N,N'-DISUBSTITUTED UREA IN THE REACTION OF PEPTIDE BOND FORMATION BY THE CARBODIIMIDE METHOD. III. REACTIONS OF STERICALLY HINDERED AMINO ACIDS AND AMINO ACIDS WITH FUNCTIONAL GROUPS IN THE SIDE CHAIN.

Author
IZDEBSKI J; KUBIAK T; KUNCE D; DRABAREK S
INST. FUNDAM. CHEM., UNIV., 02093 WARSZAWA
Source
POLISH J. CHEM.; POLAND; DA. 1978; VOL. 52; NO 3; PP. 539-545; ABS. POL.; BIBL. 10 REF.
Document type
Article
Language
English
Keyword (fr)
ACYLATION POUVOIR ROTATOIRE PROPRIETE OPTIQUE GLYCINE,ESTER ETHYLE ALPHA -AMINOACIDE(N-BENZYLOXYCARBONYL) UREE(DICYCLOHEXYL-1,3) DIPEPTIDE(N-BENZYLOXYCARBONYL) ESTER ETHYLE GLYCINE(ALPHA -BENZYLOXYCARBONYLAMINOACYL) ESTER ETHYLE UREE(ALPHA -AMINOACYL-1 DICYCLOHEXYL-1,3) CARBODIIMIDE(DICYCLOHEXYL) THF METHANE(DICHLORO) CHIMIE ORGANIQUE
Keyword (en)
ACYLATION ROTATORY POWER OPTICAL PROPERTIES DICHLOROMETHANE 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
PASCAL7860360197

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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