- P-ISSN 2233-4203
- E-ISSN 2093-8950
- Apply for Authority
- P-ISSN2233-4203
- E-ISSN2093-8950
Article Detail
Home > Article Detail
Observations on Fragmentation Pathway of Farinomalein and its Isomers by Structural Investigation Using LC-MS/MS
Mass Spectrometry Letters / Mass Spectrometry Letters, (P)2233-4203; (E)2093-8950
2018, v.9 no.1, pp.37-40
https://doi.org/10.5478/MSL.2017.9.1.37
(Affiliated to Shivaji University)
(Affiliated to Savitribai Phule Pune University)
(Affiliated to Savitribai Phule Pune University)
(Affiliated to Savitribai Phule Pune University)
(Affiliated to Savitribai Phule Pune University)
(Affiliated to Savitribai Phule Pune University)
(Affiliated to Savitribai Phule Pune University)
Firke,
N. P., Markandeya,
A. G., Konde Deshmukh,
R. S., &
Pingale,
S.
S.
(2018). Observations on Fragmentation Pathway of Farinomalein and its Isomers by Structural Investigation Using LC-MS/MS. Mass Spectrometry Letters, 9(1), 37-40, https://doi.org/10.5478/MSL.2017.9.1.37
- Downloaded
- Viewed
Abstract
Farinomalein is a maleimide-bearing compound well known for its anti-fungal activity. In the present study, synthesis of farinomalein is achieved via Stobbe condensation followed by Haval-Argade contrathermodynamic rearrangement. Kinetically driven Stobbe condensation followed by condensation with beta-alanine reveals formation of two isomers of farinomalein. This article describes application of LC-MS/MS in structure elucidation of farinomalein 1 and its isomers 2 and 3 encountered in its synthesis. The proposed distinct fragmentation pathway is supported by rational organic reaction mechanism. These fragmentation pathways are significant for analytical method development of farinomalein in near future. The structures of farinomalein 1 and its isomers 2 and 3 have been assigned undisputedly.
- keywords
- Maleimide, Stobbe condensation, Haval-Argade contrathermodynamic rearrangement, Isofarinomalein
Reference
1
2
Miles, W. H.. (2010). . Tetrahedron Lett., 51, 1710-. http://dx.doi.org/10.1016/j.tetlet.2010.01.083.
3
Aiwale, S. T.. (2012). . Syn. Comm., 43, 1455-.
4
Lahore, S.. (2014). . Tetrahedron Lett., 55, 4196-4198. http://dx.doi.org/10.1016/j.tetlet.2014.05.023.
5
Rinehart, K. L.. (1965). . J. Am. Chem. Soc., 87, 4407-.
6
Biemann, K.. (2015). . Annu. Rev. Ana. Chem., 8, 1-. http://dx.doi.org/10.1146/annurev-anchem-071114-040110.
7
Kinghorn A.. (2015). Progress in the Chemistry of Organic Natural Products 100:Springer International Publishing.
8
9
10
Banerjee, S.. (2009). . Indian J. Chem., 48B, 882-.
11
12
- Submission Date
- 2017-11-21
- Revised Date
- 2017-12-27
- Accepted Date
- 2018-01-10
Other articles from this issue
- Recent Progress on Microfluidic Electrophoresis Device Application in Mass Spectrometry
- Structural Analysis of [Cu(II)-amyloidogenic peptide] Complexes
- DC23, a Triazolothione Resorcinol Analogue, Is Extensively Metabolized to Glucuronide Conjugates in Human Liver Microsomes
- Direct Quantitation of Amino Acids in Human Serum Using a Stepwise- Dilution Strategy and a Mixed-Mode Liquid Chromatography-Tandem Mass Spectrometry Method
- Observations on Fragmentation Pathway of Farinomalein and its Isomers by Structural Investigation Using LC-MS/MS
- more
Recommanded Articles
This website recommended the use the Chrome browser for journal website.