Zobrazeno 1 - 10
of 213
pro vyhledávání: '"Radha Krishna, Palakodety"'
Publikováno v:
In Tetrahedron: Asymmetry 30 June 2013 24(12):758-763
Autor:
Sayantan Sengupta, Jala Ranjith Reddy, Nomula Rajesh, Ashish Jaiswal, Ulaganathan Mabalirajan, Radha Krishna Palakodety, Pulok Mukherjee, Arun Bandyopadhyay
Publikováno v:
European journal of pharmacology. 931
Neutrophil elastase, a powerful physiological defence tool, may serve as drug target for diverse diseases due to its bystander effect on host cells like chronic obstructive pulmonary disease (COPD). Here, we synthesised seven novel benzoxazinone deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::987d39f141030c0aa2eac67f7cfb2e15
https://pubmed.ncbi.nlm.nih.gov/35952844
https://pubmed.ncbi.nlm.nih.gov/35952844
Publikováno v:
In Tetrahedron: Asymmetry 31 May 2012 23(10):769-774
Publikováno v:
Tetrahedron Letters. 60:1978-1981
Pd/Cu-catalyzed Heck type cross-coupling reaction of p-toluenesulfonylmethyl isocyanide (TosMIC) with various styrenes to access stilbenes in DMSO solvent under mild conditions is developed. This efficient and simple approach employs TosMIC as an ary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4da26bdd95c13b77d75c754e73955336
https://doi.org/10.1016/j.tetlet.2019.06.045
https://doi.org/10.1016/j.tetlet.2019.06.045
Autor:
Ranjith Jala, Radha Krishna Palakodety
Publikováno v:
Tetrahedron Letters. 60:1437-1440
C H bond functionalization for C N and C C bond formations via cross-dehydrogenative coupling (CDC) of N-allylbenzamides with indole as amine source has been developed under a copper-catalyzed condition. To the best of our knowledge, these are the fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71460ad41f552e28041f017e6d15640e
https://doi.org/10.1016/j.tetlet.2019.04.041
https://doi.org/10.1016/j.tetlet.2019.04.041
Publikováno v:
Organic & Biomolecular Chemistry. 17:3714-3717
An easy and efficient approach to the synthesis of N,4-disubstituted quinazoline-2-amine and oxides is described. This transformation proceeds smoothly in the presence of molecular iodine. The metal-free protocol presented here is insensitive to air
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f31cf50534cfe0ea7c5f1acd8ff82b0a
https://doi.org/10.1039/c9ob00349e
https://doi.org/10.1039/c9ob00349e
Publikováno v:
In Tetrahedron Letters 30 January 2020 61(5)
Publikováno v:
Advanced Synthesis & Catalysis. 360:2806-2812
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::027ef7638c7a07a65331d83a055144ae
https://doi.org/10.1002/adsc.201800353
https://doi.org/10.1002/adsc.201800353
Publikováno v:
The Journal of Organic Chemistry. 83:5715-5723
An environmentally benign and convenient strategy for the synthesis of 4,5-disubstituted/N-fused 3-amino-1,2,4-triazoles and 3-substituted 5-amino-1,2,4-thiadiazoles from isothiocyanates has been developed. This metal-free method involves I2-mediated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a53c97eddf43f5cb13a8ab09234e432b
https://doi.org/10.1021/acs.joc.8b00753
https://doi.org/10.1021/acs.joc.8b00753
Publikováno v:
In Tetrahedron: Asymmetry 2007 18(18):2197-2200