Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Mangarao, Nakka"'
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
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:
Advanced Synthesis & Catalysis. 358:520-525
A convenient and efficient protocol has been developed for the synthesis of 1,2,4-triazoles, N-fused 1,2,4-triazoles and 1,2,4-oxadiazoles using molybdenum hexacarbonyl where, for the first time, molybdenum hexacarbonyl acts as a convenient and relia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd521e5c7e150765cdbc0ca9d0ed7f2f
https://doi.org/10.1002/adsc.201500703
https://doi.org/10.1002/adsc.201500703
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
Akademický článek
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Publikováno v:
European Journal of Organic Chemistry. 2015:5929-5933
The facile and efficient one-pot construction of benzimidazoles and benzoxazoles through the Mo(CO)6-mediated carbonylation of aryl halides was examined. In the process, Mo(CO)6 acted as a convenient and safe solid source of carbon monoxide. A wide r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::927b8da2bef80d0e36fdb780fee95aa0
https://doi.org/10.1002/ejoc.201500803
https://doi.org/10.1002/ejoc.201500803
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
Autor:
Ramu Tadikonda, Prasanthi Sarakula, Srinuvasarao Rayavarapu, Mangarao Nakka, Siddaiah Vidavalur
Publikováno v:
Synthesis. 47:517-525
An environmentally benign protocol is described for the synthesis of 3,4,5-trisubstituted 1,2,4-triazoles and N-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones and aldehydes using polyethylene glycol as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22447857c72d477123b9413c86ee8777
https://doi.org/10.1055/s-0034-1378909
https://doi.org/10.1055/s-0034-1378909
Autor:
Ramu Tadikonda, Mahaboob Basha Gajula, Srinuvasarao Rayavarapu, Siddaiah Vidavalur, Mangarao Nakka, Padma Rao Gollamudi
Publikováno v:
Synthetic Communications. 44:1978-1986
Silica-supported perchloric acid (HClO4-SiO2) was found to be a new, highly efficient, inexpensive, and reusable catalyst for a rapid and efficient synthesis of various 1,2,4-oxadiazoles with good to excellent yields under solvent-free conditions. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84f13598adac23e9f7f4a4c5dc3f18ad
https://doi.org/10.1080/00397911.2014.883633
https://doi.org/10.1080/00397911.2014.883633