Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ashok Konala"'
Autor:
Ching Fa Yao, Zonghan Yang, Veerababurao Kavala, Ashok Konala, Jian Yao Ruan, Chun Wei Kuo, Tang Hao Yang
Publikováno v:
European Journal of Organic Chemistry. 2018:1241-1247
Autor:
Ching Fa Yao, Veerababurao Kavala, Trimurtulu Kotipalli, Ashok Konala, Chun Wei Kuo, Che Hao Hsu, Vijayalakshmi Bandi, Bharath Kumar Villuri
Publikováno v:
RSC Adv.. 7:46704-46712
An approach for the synthesis of functionalized unsymmetrical 1,3-butadiene-3-yne derivatives is reported starting from β-halo styrene and phenyl acetylene derivatives in the presence of PdCl2 and CuI catalysts. Functional groups such as aldehyde, c
Publikováno v:
Chemical Communications. 53:1676-1679
A metal-free protocol for accessing both α and δ-carboline derivatives, starting from a common indolylchalcone oxime ester precursor is reported. The reaction involves mild conditions and uses a regiodivergent approach. DDQ is used as a switching a
Autor:
Trimurtulu Kotipalli, Donala Janreddy, Ashok Konala, Ching Fa Yao, Veerababurao Kavala, Chu Wei Kuo
Publikováno v:
Advanced Synthesis & Catalysis. 358:2652-2660
Autor:
Veerababurao Kavala, Yu Wen Chen, Chun Wei Kuo, Lyu Lin, Ashok Konala, Chia Yu Huang, Tang Hao Yang, Ching Fa Yao
Publikováno v:
RSC Advances. 6:96049-96056
3-Arylindole derivatives were synthesized by Cu(I) catalysed intramolecular Ullmann coupling of 2-bromoarylaminoalkanes. 2-Bromoarylaminoalkanes were synthesized from 2-bromoarylnitroalkanes, which in turn prepared through AlCl3-mediated Friedel–Cr
Autor:
Sabbasani Rajasekhara Reddy, Ching Fa Yao, Ashok Konala, Lichun Lin, Veerababurao Kavala, Chun Wei Kuo, Bharath Kumar Villuri, Vijayalakshmi Bandi, Che Hao Hsu
Publikováno v:
The Journal of organic chemistry. 84(6)
An efficient method for the synthesis of polysubstituted cyclopentene and cyclopenta[ b]carbazole derivatives through the iodine-promoted electrocyclization of substituted indoles and 4-arylidene-3,6-diarylhex-2-en-5-ynal derivatives is reported. Pol
Autor:
Salawu O. Adio, Saeed S. Albaseer, Ahmad Aqel, Chandra S. Bhatt, Krishna Bisetty, Carla Beatriz Grespan Bottoli, Rani Bushra, Meire Ribeiro da Silva, Shilpee Sachar, Armando C. Duarte, Bruno Henrique Fumes, Mariana Roberto Gama, Chandraiah Godugu, Javier González-Sálamo, Farideh Haghighi, Bahrudeen S. Hameed, Javier Hernández-Borges, Antonio V. Herrera-Herrera, Chaudhery Mustansar Hussain, Mohammad S. Hussain, Celine I.L. Justino, Suvardhan Kanchi, Rustem Kecili, Amit Khurana, Ashok Konala, Fernando Mauro Lanças, Surinder Kumar Mehta, Sonia Morante-Zarcero, Carlos Eduardo Domingues Nazario, Bharathkumar Nagaraj, Ramisetti Nageswara Rao, Mazen Kumar Nazal, Amir Sanati-Nezhad, Ankush Parmar, Krystyna Pyrzynska, Teresa A.P. Rocha-Santos, Mohd A. Saifi, Muhammad Sajid, Shweta Sharma, Isabel Sierra, Bárbara Socas-Rodríguez, Anil K. Suresh, Zahra Talebpour, Kishore K.R. Tetala
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecaf69fb71c16f946e46f3f830f7f905
https://doi.org/10.1016/b978-0-12-812792-6.00026-1
https://doi.org/10.1016/b978-0-12-812792-6.00026-1
Autor:
Ashok Konala, Kishore K.R. Tetala
Rapid, efficient separation and accurate identification of valuable biomolecules like nucleic acids, proteins, and polysaccharides from complex mixtures like serum, milk, and plant extracts require reliable analytical tools [1]. The degree of complex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::000f4c858cd8663f41ba4027fcfdb935
https://doi.org/10.1016/b978-0-12-812792-6.00011-x
https://doi.org/10.1016/b978-0-12-812792-6.00011-x
Publikováno v:
The Journal of organic chemistry. 82(14)
An efficient approach for the synthesis of benzo-fused pyridoindolone derivatives via a one-pot copper catalyzed tandem reaction of 2-iodobenzamides with 2-iodobenzylcyanides has been developed. Using this protocol, benzo-fused pyridoindolone derivat
Publikováno v:
Chem. Commun.. 50:15124-15135
This review describes the development in the use of Au(I)/Brønsted acid binary catalytic systems to enable an enantioselective transformation in one-pot that cannot be achieved by gold catalysts alone. The examples discussed herein are promising sin