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pro vyhledávání: '"Trimurtulu Kotipalli"'
Autor:
TRIMURTULU KOTIPALLI, 柯帝
104
The contents of this dissertation is divided into two parts (Part I, Part II). Part Ι is subdivided into four sections i.e. Section A, B, C, D. Section A, illustrates the overview on 2-halo N-substituted benzamide derivatives. this section
The contents of this dissertation is divided into two parts (Part I, Part II). Part Ι is subdivided into four sections i.e. Section A, B, C, D. Section A, illustrates the overview on 2-halo N-substituted benzamide derivatives. this section
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/63846157330424238004
Publikováno v:
Organic & Biomolecular Chemistry. 19:10390-10402
Bromotrimethylsilane (TMSBr)-promoted intramolecular cyclization of (o-arylethynyl)benzyl ethers to form 1H-isochromenes at room temperature is reported. Further studies indicated that vinyl carbocations are the reaction intermediates which are stabi
Publikováno v:
Organicbiomolecular chemistry. 19(47)
Bromotrimethylsilane (TMSBr)-promoted intramolecular cyclization of (
Autor:
Duen Ren Hou, Trimurtulu Kotipalli
Publikováno v:
Asian Journal of Organic Chemistry. 8:1561-1571
Autor:
Trimurtulu Kotipalli, Duen Ren Hou
Publikováno v:
Organic Letters. 20:4787-4790
A new and efficient protocol to prepare indenes is reported. Assisted by boron trifluoride diethyl etherate, the one-pot reaction of aryl homopropargyl alcohols and aldehydes in the presence of arenes yielded indene derivatives. The reaction was stud
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
Autor:
Trimurtulu Kotipalli, Donala Janreddy, Ashok Konala, Ching Fa Yao, Veerababurao Kavala, Chu Wei Kuo
Publikováno v:
Advanced Synthesis & Catalysis. 358:2652-2660
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
Autor:
Sachin S. Ichake, Bharath Kumar Villuri, Veerababurao Kavala, Trimurtulu Kotipalli, Ching Fa Yao, Chun Wei Kuo, Vijayalakshmi Bandi
Publikováno v:
RSC Advances. 6:74845-74858
Copper catalyzed C-terminal and N-terminal attack of 2-alkynylanilines to 2-iodobenzamides afforded isoindolinones and 1,2-disubstituted indoles, respectively. Further, the isoindolinone derivatives were converted to spiro fused isoindolinone-indolin
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