-
Je něco špatně v tomto záznamu ?
Base-mediated intramolecular C- and N-arylation of N,N-disubstituted 2-nitrobenzenesulfonamides: advanced intermediates for the synthesis of diverse nitrogenous heterocycles
P. Smyslová, K. Kisseljova, V. Krchňák,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25076047
DOI
10.1021/co5000739
Knihovny.cz E-zdroje
- MeSH
- dusík chemie MeSH
- dusíkaté sloučeniny chemie MeSH
- heterocyklické sloučeniny chemická syntéza chemie MeSH
- molekulární struktura MeSH
- sulfonamidy chemie MeSH
- uhlík chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Structural and electronic features that facilitate and direct the intramolecular C- and N-arylation of 2-alkyl-2-{[N-(benzyl)-2-nitrophenyl]sulfonamido}acetic acid esters and amides were examined. The substitution pattern and amino acid carboxy-terminal functionality determined the arylation position. C/N-arylated products represent advanced intermediates for combinatorial synthesis of diverse nitrogenous heterocycles, including indazoles, quinazolinones, quinoxalinones, and 3-amino-2-oxindoles.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15023190
- 003
- CZ-PrNML
- 005
- 20150709122804.0
- 007
- ta
- 008
- 150709s2014 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1021/co5000739 $2 doi
- 035 __
- $a (PubMed)25076047
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Smyslová, Petra $u Department of Organic Chemistry, Institute of Molecular and Translational Medicine, Faculty of Science, Palacký University , 17. Listopadu 12, 771 46 Olomouc, Czech Republic.
- 245 10
- $a Base-mediated intramolecular C- and N-arylation of N,N-disubstituted 2-nitrobenzenesulfonamides: advanced intermediates for the synthesis of diverse nitrogenous heterocycles / $c P. Smyslová, K. Kisseljova, V. Krchňák,
- 520 9_
- $a Structural and electronic features that facilitate and direct the intramolecular C- and N-arylation of 2-alkyl-2-{[N-(benzyl)-2-nitrophenyl]sulfonamido}acetic acid esters and amides were examined. The substitution pattern and amino acid carboxy-terminal functionality determined the arylation position. C/N-arylated products represent advanced intermediates for combinatorial synthesis of diverse nitrogenous heterocycles, including indazoles, quinazolinones, quinoxalinones, and 3-amino-2-oxindoles.
- 650 _2
- $a uhlík $x chemie $7 D002244
- 650 _2
- $a heterocyklické sloučeniny $x chemická syntéza $x chemie $7 D006571
- 650 _2
- $a molekulární struktura $7 D015394
- 650 _2
- $a dusíkaté sloučeniny $x chemie $7 D009574
- 650 _2
- $a dusík $x chemie $7 D009584
- 650 _2
- $a sulfonamidy $x chemie $7 D013449
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kisseljova, Ksenija
- 700 1_
- $a Krchňák, Viktor
- 773 0_
- $w MED00179493 $t ACS combinatorial science $x 2156-8944 $g Roč. 16, č. 9 (2014), s. 500-5
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25076047 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20150709 $b ABA008
- 991 __
- $a 20150709122824 $b ABA008
- 999 __
- $a ok $b bmc $g 1083528 $s 906183
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 16 $c 9 $d 500-5 $i 2156-8944 $m ACS combinatorial science $n ACS comb. sci. $x MED00179493
- LZP __
- $a Pubmed-20150709
