Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nagesh, Jatangi"'
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:
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
Autor:
Sridhar Balasubramanian, Nagaraju Tumula, Nagesh Jatangi, Radha Krishna Palakodety, Mangarao Nakka
Publikováno v:
The Journal of Organic Chemistry. 82:5310-5316
A novel and expeditious approach for the synthesis of N-fused and 3,4-disubstituted 5-imino-1,2,4-thiadiazole derivatives has been achieved through the molecular iodine-catalyzed oxidative cyclization of 2-aminopyridine/amidine and isothiocyanate via
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::185fa303720dd8bf17cdd0a7f2031e54
https://doi.org/10.1021/acs.joc.7b00646
https://doi.org/10.1021/acs.joc.7b00646
Publikováno v:
Organicbiomolecular chemistry. 17(15)
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=pmid________::5baecfeb91d961d858faf280ed5f8604
https://pubmed.ncbi.nlm.nih.gov/30882837
https://pubmed.ncbi.nlm.nih.gov/30882837
Publikováno v:
The Journal of organic chemistry. 83(10)
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 I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0cdf77226868d7673a77c64a9f9330e7
https://pubmed.ncbi.nlm.nih.gov/29717614
https://pubmed.ncbi.nlm.nih.gov/29717614
Autor:
Nagaraju, Tumula, Nagesh, Jatangi, Radha Krishna, Palakodety, Sridhar, Balasubramanian, Mangarao, Nakka
Publikováno v:
The Journal of organic chemistry. 82(10)
A novel and expeditious approach for the synthesis of N-fused and 3,4-disubstituted 5-imino-1,2,4-thiadiazole derivatives has been achieved through the molecular iodine-catalyzed oxidative cyclization of 2-aminopyridine/amidine and isothiocyanate via
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ebe102e4f9e78e167397d067917fbbc5
https://pubmed.ncbi.nlm.nih.gov/28447462
https://pubmed.ncbi.nlm.nih.gov/28447462
Publikováno v:
Tetrahedron Letters. 60:151186
An alternative green protocol and step economy for the synthesis of quinazoline has been developed. The reaction of readily available 2-aminobenzonitriles with various organometallic reagents led to ortho-aminoaryl N H ketimine species. The subsequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5e1b21a13f63b26cccccc978fc673c7
https://doi.org/10.1016/j.tetlet.2019.151186
https://doi.org/10.1016/j.tetlet.2019.151186