Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Donala, Janreddy"'
Autor:
Barange, Deepak Kumar, Kavala, Veerababurao, Kuo, Chun-Wei, Wang, Cheng-Chuan, Rajawinslin, R.R., Donala, Janreddy, Yao, Ching-Fa
Publikováno v:
In Tetrahedron 14 October 2014 70(41):7598-7605
Autor:
Trimurtulu Kotipalli, Donala Janreddy, Ashok Konala, Ching Fa Yao, Veerababurao Kavala, Chu Wei Kuo
Publikováno v:
Advanced Synthesis & Catalysis. 358:2652-2660
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ee35a5a0dd600ed32bd17083c26ea53
https://doi.org/10.1002/adsc.201600274
https://doi.org/10.1002/adsc.201600274
Autor:
Trimurtulu Kotipalli, Veerababurao Kavala, Chun Wei Kuo, Vijayalakshmi Bandi, Ching Fa Yao, Donala Janreddy
Publikováno v:
European Journal of Organic Chemistry. 2016:1182-1193
The synthesis of quinazolinone derivatives was achieved from 2-iodobenzamide derivatives and various benzylamines, allylamine, and cinnamylamine derivatives through a one-pot copper-catalyzed reaction. In this reaction, the amine component (benzylami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c34a44a137f5eace40636ab70e2314c
https://doi.org/10.1002/ejoc.201501552
https://doi.org/10.1002/ejoc.201501552
Publikováno v:
Israel Journal of Chemistry. 55:347-359
In recent years, there has been rapid expansion of glycan synthesis, fueled by the recognition that the structural complexity of sugars translates to a myriad of biological functions. Such chemical syntheses involve many challenges, mostly due to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d4d9147ca4e0eb4b61000d79854e51c
https://doi.org/10.1002/ijch.201400171
https://doi.org/10.1002/ijch.201400171
Autor:
Chun Wei Kuo, Ting Shen Kuo, Ching Fa Yao, R. R. Rajawinslin, Mei Ling Chen, Veerababurao Kavala, Mustafa J. Raihan, Donala Janreddy, Chiu Hui He
Publikováno v:
Tetrahedron. 70:7505-7510
A Selectfluor and base mediated protocol for the synthesis of cyclohexanone ring fused isoxazole derivatives from isoxazoline N-oxides has been successfully developed. This rapid, one-pot, two-step transformation is achieved in acetonitrile, through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02911a447ce9789d758341b8608da9e7
https://doi.org/10.1016/j.tet.2014.08.024
https://doi.org/10.1016/j.tet.2014.08.024
Autor:
Donala Janreddy, Ching Fa Yao, Trimurtulu Kotipalli, Ting Shen Kuo, Veerababurao Kavala, Chiu Hui He, Mei Ling Chen, Chun Wei Kuo
Publikováno v:
Advanced Synthesis & Catalysis. 356:3083-3091
We describe a simple and efficient synthetic methodology for the synthesis of a library of 2,4dicarbonyl-substituted naphthalene derivatives through the PdCl2-catalyzed aerobic oxidative intermolecular cycloaddition of 2-alkynylbenzaldehydes to some
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bc70769028c79f7e41593ee5b85b8c2
https://doi.org/10.1002/adsc.201400180
https://doi.org/10.1002/adsc.201400180
Autor:
Hsiu Ni Huang, Donala Janreddy, Veerababurao Kavala, Trimurtulu Kotipalli, Ching Fa Yao, Chiu Hui He, Ting Shen Kuo, Chun Wei Kuo
Publikováno v:
RSC Advances. 4:2274-2283
The synthesis of indolo[1,2-a]quinazolinone starting from 2-iodobenzamide and indole derivatives is reported. In this two-step procedure, indole is N-arylated with 2-iodobenzamide derivatives via Ullman coupling, followed by an intramolecular C–H a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::632681e044200d8341b90eb17c098ceb
https://doi.org/10.1039/c3ra44798g
https://doi.org/10.1039/c3ra44798g
Autor:
Ting Shen Kuo, Mei Ling Chen, Chiu Hui He, Donala Janreddy, Veerababurao Kavala, Trimurtulu Kotipalli, Chun Wei Kuo, Ching Fa Yao
Publikováno v:
RSC Adv.. 4:47833-47840
A simple and efficient one pot protocol was developed for the synthesis of new structurally diverse 10-indolyldibenzo[b,f]azepine derivatives. The reaction involves Lewis-acid mediated ring expansion followed by C–C bond formation through nucleophi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa5be44375f20a02d2f4676ed1799f68
https://doi.org/10.1039/c4ra08723b
https://doi.org/10.1039/c4ra08723b
Autor:
Trimurtulu Kotipalli, Veerababurao Kavala, Ching Fa Yao, Wen Chang Chen, Mei Ling Chen, Ting Shen Kuo, Chiu Hui He, Chun Wei Kuo, Donala Janreddy, Chintakunta Ramesh
Publikováno v:
Advanced Synthesis & Catalysis. 355:2918-2927
A novel, copper(I)-promoted azide-alkene aerobic oxidative cycloaddition protocol was devel- oped for the regioselective synthesis of 1,4-disubsti- tuted/1,4,5-trisubstituted 1,2,3-triazoles by using azides and electron-deficient olefins under an oxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c2404c224378d946be43f54dfdc054f
https://doi.org/10.1002/adsc.201300344
https://doi.org/10.1002/adsc.201300344
Autor:
Ching Fa Yao, Mustafa J. Raihan, Veerababurao Kavala, Mei Ling Chen, Chun Wei Kuo, Donala Janreddy, Chiu Hui He, Ting Shen Kuo, R. R. Rajawinslin
Publikováno v:
European Journal of Organic Chemistry. 2013:5743-5749
A rapid method for the synthesis of long-chain fluorinated compounds using a C–C bond-cleavage reaction was developed. Selectfluor was the most effective fluorinating agent of those tested in this study. Long-chain fluoro dioxo nitriles were formed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c74b3876c4ef23997c4bb620bd248867
https://doi.org/10.1002/ejoc.201300599
https://doi.org/10.1002/ejoc.201300599