scholarly journals Ureido Derivatives of Neoabietic Acid

Molbank ◽  
10.3390/m1033 ◽  
2018 ◽  
Vol 2018 (4) ◽  
pp. M1033
Author(s):  
Xinyu Gao ◽  
Niping Feng ◽  
Yuhan Zi ◽  
Jianguo Cao ◽  
Guozheng Huang
Keyword(s):  
Spectral Analysis ◽  
1H Nmr ◽  
13C Nmr ◽  
Structure Characterization ◽  
Curtius Rearrangement ◽  
Neoabietic Acid ◽  
Rearrangement Reaction ◽  
Derivatives Of

A series of ureido derivatives of neoabietic acid were synthesized by application of Curtius rearrangement reaction to neoabietic acid and amines. Structure characterization of these compounds was done by 1H-NMR, 13C-NMR and HRMS spectral analysis.

scholarly journals 3-(3,5-Difluorophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde

Molbank ◽  
10.3390/m1011 ◽  
2018 ◽  
Vol 2018 (3) ◽  
pp. M1011 ◽  
Author(s):  
Naveen Kumar ◽  
Swamy Sreenivasa ◽  
Vasantha Kumar ◽  
Nadigar Mohan
Keyword(s):  
Spectral Analysis ◽  
1H Nmr ◽  
13C Nmr ◽  
High Purity ◽  
Title Compound ◽  
Good Yield ◽  
Phosphorus Oxychloride ◽  
Structure Characterization ◽  
Dimethyl Formamide

Vilsmeier–Haack reaction of (E)-1-[1-(3,5-difluorophenyl)ethylidene]-2-phenylhydrazine (1) using dimethyl formamide in excess of phosphorus oxychloride by conventional method, resulted in the synthesis of the title compound 3-(3,5-difluorophenyl)-1-phenyl-1H-pyrazole-4- carbaldehyde (2) in good yield and high purity. Structure characterization of the title compound was done by IR, 1H-NMR, 13C-NMR and HRMS spectral analysis.

scholarly journals 1-Methyl-3-{4-[(4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl)benzyl]}-2-phenylindole

Molbank ◽  
10.3390/m1023 ◽  
2018 ◽  
Vol 2018 (4) ◽  
pp. M1023 ◽  
Author(s):  
Jean Guillon ◽  
Solène Savrimoutou ◽  
Sandra Rubio ◽  
Vanessa Desplat
Keyword(s):  
Spectral Analysis ◽  
Cell Lines ◽  
13C Nmr ◽  
Title Compound ◽  
Indole Derivative ◽  
Leukemia Cell ◽  
Structure Characterization ◽  
Cytotoxic Potential ◽  
Leukemia Cell Lines

The 1-methyl-3-{4-[(4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl)benzyl]}-2-phenylindole compound has been successfully synthesized via a multistep pathway starting from 2-phenylindole. Structure characterization of this new indole derivative was done by FTIR, 1H-NMR, 13C-NMR, and HRMS spectral analysis. The title compound showed high cytotoxic potential against five leukemia cell lines (K562, HL60, U937, U266, and Jurkat cell lines).

scholarly journals 3-(3,5-Difluorophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde

2018 ◽  
Author(s):  
Naveen Kumar ◽  
Swamy Sreenivasa ◽  
Vasantha Kumar ◽  
Nadigar Revansiddappa Mohan
Keyword(s):  
Spectral Analysis ◽  
13C Nmr ◽  
Title Compound ◽  
Structure Characterization ◽  
Dimethyl Formamide ◽  
The Novel ◽  
Mass Spectral Analysis ◽  
Mass Spectral ◽  
Phosphorous Oxychloride

Vilsmeier–Haack reaction of (E)-1-(1-(3,5-difluorophenyl)ethylidene)-2-phenylhydrazine (1) using dimethyl formamide in excess of phosphorous oxychloride by conventional method, resulted in the synthesis of title compound 3-(3,5-difluorophenyl)-1-phenyl-1H-pyrazole-4- carbaldehyde (2) in good yield and high purity. Structure characterization of the novel title compound was done by IR, 1H NMR, 13C NMR and mass spectral analysis.

Synthesis and Spectral Characterization of New S-Alkylated 1,2,4-Triazoles as Potential Biological Agents

2017 ◽  
Vol 68 (10) ◽  
pp. 2436-2439
Author(s):  
Stefania Felicia Barbuceanu ◽  
Laura Ileana Socea ◽  
Constantin Draghici ◽  
Elena Mihaela Pahontu ◽  
Theodora Venera Apostol ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Spectral Data ◽  
1H Nmr ◽  
Elemental Analysis ◽  
13C Nmr ◽  
Ethyl Bromide ◽  
Spectral Characterization ◽  
Basic Medium ◽  
Phenacyl Bromide

In the work we presented the behavior of 5-(4-(4-X-phenylsulfonyl)phenyl)-4-(n-propyl)-2H-1,2,4-triazole-3(4H)-thiones (X= Cl or Br) with some alkylation agents. Thus, new S-alkylated 1,2,4-triazole derivatives were synthesized by reaction of the corresponding 1,2,4-triazole-3-thione derivatives with different �-halogenated compounds (ethyl bromide, ethyl chloroacetate or phenacyl bromide), in basic medium. The structures of synthesized compounds were elucidated by spectral data (1H-NMR, 13C-NMR, mass spectrometry) and elemental analysis.

Combined High-Resolution Solid-State 1H/13C NMR Spectroscopy and 1H NMR Relaxometry for the Characterization of Kerogen Thermal Maturation

2020 ◽  
Author(s):  
Francesco Panattoni ◽  
Jonathan Mitchell ◽  
Edmund J. Fordham ◽  
Ravinath Kausik ◽  
Clare P. Grey ◽  
...  
Keyword(s):  
Solid State ◽  
Nmr Spectroscopy ◽  
High Resolution ◽  
1H Nmr ◽  
13C Nmr ◽  
13C Nmr Spectroscopy ◽  
Thermal Maturation ◽  
Nmr Relaxometry ◽  
1H Nmr Relaxometry

Synthesis and Characterization of N-butyl-N-methylimidazolium- D-(-)-tartrate Chiral Ionic Liquid

2012 ◽  
Vol 518-523 ◽  
pp. 3989-3992 ◽  
Author(s):  
Yang Zhang ◽  
Xiao Hua Tu ◽  
Cheng Ping Miao ◽  
Jian Yi Wu
Keyword(s):  
Ionic Liquid ◽  
1H Nmr ◽  
Ion Chromatography ◽  
13C Nmr ◽  
Nmr Spectra ◽  
Optical Rotation ◽  
Synthesis And Characterization ◽  
13C Nmr Spectra ◽  
Chiral Ionic Liquid

A novel CIL of N-butyl-N-methyl imidazolium-D-(-)-tartrate has been designed and synthesized by neutralization reaction. Its structure was characterized by 1H-NMR and 13C-NMR spectra, the optical rotation was characterized by polarimeter with the value of-15.0º, and the purity was characterized by ion chromatography with the value of 98.4%.

Synthesis and Characterization of Some 4- Substituted Thiazolidinone Derivatives

2019 ◽  
Vol 10 (04) ◽  
pp. 631-636
Author(s):  
Zainab Ryad Magtoof ◽  
Mahmood Shakir Magtoof
Keyword(s):  
Schiff Bases ◽  
1H Nmr ◽  
13C Nmr ◽  
Mercaptoacetic Acid ◽  
Spectral Studies ◽  
Synthesis And Characterization

This study is concerned with the synthesis and characterization of 4-thiazolidinone derivatives (3a-3e). These compounds were prepared by reacting mercaptoacetic acid with the appropriate Schiff bases (imines) by heating at 50-60 °C in chloroform with moderate yields (51- 75 %). The structures of these 4-thiazolidinone derivatives were established on the basis of spectral studies using IR, 1H-NMR, 13C-NMR, and13C-NMR DEPT .

1H NMR and 13C NMR characterization of n-heptane extraction of low-temperature coal tar reacted with formaldehyde

2019 ◽  
Vol 42 (12) ◽  
pp. 1490-1498
Author(s):  
Qiuxiang Yao ◽  
Xiangxi Kong ◽  
Xiaomin Dai ◽  
Junwen Gao ◽  
Rucheng Wang ◽  
...  
Keyword(s):  
Low Temperature ◽  
1H Nmr ◽  
13C Nmr ◽  
Coal Tar ◽  
Nmr Characterization

scholarly journals Characterization of the Polycondensation by 1H NMR and 13C NMR

1998 ◽  
Vol 71 (7) ◽  
pp. 420-425
Author(s):  
Chikara KAWAMURA ◽  
Kenjiro TSUBOUCHI
Keyword(s):  
1H Nmr ◽  
13C Nmr

scholarly journals Complete 1H-NMR and 13C-NMR spectral analysis of the pairs of 20(S) and 20(R) ginsenosides

2014 ◽  
Vol 38 (3) ◽  
pp. 194-202 ◽  
Author(s):  
Heejung Yang ◽  
Jeom Yong Kim ◽  
Sun Ok Kim ◽  
Young Hyo Yoo ◽  
Sang Hyun Sung
Keyword(s):  
Spectral Analysis ◽  
1H Nmr ◽  
13C Nmr
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