Synthesis of methyl
2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl)
carbonylamino] alkanoates and methyl
2-[2-((1,2-dihydro-4-hydroxy-2-oxo-1-
phenylquinolin-3-yl)carbonyl-amino)alkanamido] alkanoate

J 2017

Synthesis of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl) carbonylamino] alkanoates and methyl 2-[2-((1,2-dihydro-4-hydroxy-2-oxo-1- phenylquinolin-3-yl)carbonyl-amino)alkanamido] alkanoate

FATHALA, Walid Mohamed a Pavel PAZDERA

Základní údaje

Originální název

Synthesis of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl) carbonylamino] alkanoates and methyl 2-[2-((1,2-dihydro-4-hydroxy-2-oxo-1- phenylquinolin-3-yl)carbonyl-amino)alkanamido] alkanoate

Autoři

FATHALA, Walid Mohamed (818 Egypt) a Pavel PAZDERA (203 Česká republika, garant, domácí)

Vydání

ARKIVOC, GAINESVILLE, USA, ARCAT-USA, 2017, 1551-7004

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10401 Organic chemistry

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 1.048

Kód RIV

RIV/00216224:14310/17:00097589

Organizační jednotka

Přírodovědecká fakulta

DOI

http://dx.doi.org/10.3998/ark.5550190.p009.946

UT WoS

000414746900014

Klíčová slova anglicky

Amino acid esters; DCC coupling method; azide coupling method; direct amino acid condensation; anisotropy; intramolecular hydrogen bond interactions; linomide

Štítky

NZ, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 12. 4. 2018 10:24, Ing. Nicole Zrilić

Anotace

V originále

A series of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl)carbonylamino] alkanoates 7a-f has been developed by the direct condensation of ethyl [4-hydroxy-2-oxo--1-phenyl-1,2-dihydro-3-quinoline] carboxylate 4 with amino acid ester hydrochloride in the presence of triethylamine. The quinoline amino acid esters 7a-f were the key intermediate for the preparation of a series of methyl 2-[2-((1,2-dihydro-4-hydroxy-2- oxo-1-phenylquinolin-3-yl)carbonylamino)alkanamido] alkanoate 10-13(a-f) via azide coupling method with amino acid ester.

Citovat

FATHALA, Walid Mohamed a Pavel PAZDERA. Synthesis of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl) carbonylamino] alkanoates and methyl 2-[2-((1,2-dihydro-4-hydroxy-2-oxo-1- phenylquinolin-3-yl)carbonyl-amino)alkanamido] alkanoate. ARKIVOC. GAINESVILLE, USA: ARCAT-USA, 2017, roč. 2017, č. 4, s. 158-173. ISSN 1551-7004. Dostupné z: https://dx.doi.org/10.3998/ark.5550190.p009.946.

@article{1389548,
   author = {Fathala, Walid Mohamed and Pazdera, Pavel},
   article_location = {GAINESVILLE, USA},
   article_number = {4},
   doi = {http://dx.doi.org/10.3998/ark.5550190.p009.946},
   keywords = {Amino acid esters; DCC coupling method; azide coupling method; direct amino acid condensation; anisotropy; intramolecular hydrogen bond interactions; linomide},
   language = {eng},
   issn = {1551-7004},
   journal = {ARKIVOC},
   title = {Synthesis of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl) carbonylamino] alkanoates and methyl 2-[2-((1,2-dihydro-4-hydroxy-2-oxo-1- phenylquinolin-3-yl)carbonyl-amino)alkanamido] alkanoate},
   url = {http://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/2017/4/},
   volume = {2017},
   year = {2017}
}

TY  - JOUR
ID  - 1389548
AU  - Fathala, Walid Mohamed - Pazdera, Pavel
PY  - 2017
TI  - Synthesis of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl) carbonylamino] alkanoates and methyl 2-[2-((1,2-dihydro-4-hydroxy-2-oxo-1- phenylquinolin-3-yl)carbonyl-amino)alkanamido] alkanoate
JF  - ARKIVOC
VL  - 2017
IS  - 4
SP  - 158-173
EP  - 158-173
PB  - ARCAT-USA
SN  - 15517004
KW  - Amino acid esters
KW  - DCC coupling method
KW  - azide coupling method
KW  - direct amino acid condensation
KW  - anisotropy
KW  - intramolecular hydrogen bond interactions
KW  - linomide
UR  - http://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/2017/4/
L2  - http://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/2017/4/
N2  - A series of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl)carbonylamino] alkanoates 7a-f has been developed by the direct condensation of ethyl [4-hydroxy-2-oxo--1-phenyl-1,2-dihydro-3-quinoline] carboxylate 4 with amino acid ester hydrochloride in the presence of triethylamine. The quinoline amino acid esters 7a-f were the key intermediate for the preparation of a series of methyl 2-[2-((1,2-dihydro-4-hydroxy-2- oxo-1-phenylquinolin-3-yl)carbonylamino)alkanamido] alkanoate 10-13(a-f) via azide coupling method with amino acid ester.
ER  -

FATHALA, Walid Mohamed a Pavel PAZDERA. Synthesis of methyl 2-[(1,2-dihydro-4-hydroxy-2-oxo-1-phenylquinolin-3-yl) carbonylamino] alkanoates and methyl 2-[2-((1,2-dihydro-4-hydroxy-2-oxo-1- phenylquinolin-3-yl)carbonyl-amino)alkanamido] alkanoate. \textit{ARKIVOC}. GAINESVILLE, USA: ARCAT-USA, 2017, roč.~2017, č.~4, s.~158-173. ISSN~1551-7004. Dostupné z: https://dx.doi.org/10.3998/ark.5550190.p009.946.

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