Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Muralikrishna Valluri"'
Autor:
Vijayasaradhi, Sivalenka, Muralikrishna, Valluri, Srinivas, Ravula, Rao, Cherukumalli Purna Koteswara, Prasad, Kotipalli Yesu, Prasad, Byreddy, Khanna, Baman
Publikováno v:
In Results in Chemistry January 2023 5
Autor:
Satyanarayana Tummanapalli, Kali Charan Gulipalli, Srinivas Endoori, Srinu Bodige, Anil Kumar Pommidi, Srinivas Medaboina, Swathi Rejinthala, Suresh Choppadandi, Ravi Boya, Ashok Kanuka, Muralikrishna Valluri
Publikováno v:
Tetrahedron Letters. 104:154022
Autor:
Yansong Zheng, Muralikrishna Valluri, Mitchell A. Avery, Rajashaker Kache, Panicker Bijoy, Jae-Chul Jung, Kimberly K. Vines
Publikováno v:
The Journal of Organic Chemistry. 69:9269-9284
A convergent, total synthesis of epothilones B (2) and D (4) is described. The key steps are Normant coupling to establish the desired (Z)-stereochemistry at C12-C13, Wadsworth-Emmons olefination of methyl ketone 28 with the phosphonate ester 8, dias
Publikováno v:
Tetrahedron Letters. 35:3609-3612
An elegant approach for the regioselective preparation of hydroxy butenolide by the oxidation of 2-ethoxyfuran with MnO2-HCl is described.
Publikováno v:
Tetrahedron Letters. 35:3613-3616
Publikováno v:
ChemInform. 33
Publikováno v:
ChemInform. 33
A new, mild, and chemoselective method for the deprotection of trichloroethoxylcarbonyl and trichloroacetyl groups is described.
Autor:
Muralikrishna Valluri, Kimberly K. Vines, Yansong Zheng, Mitchell A. Avery, Rajashaker Kache, Jae-Chul Jung, Panicker Bijoy
Publikováno v:
ChemInform. 36
Autor:
Mitchell A. Avery, Jae-Chul Jung, Muralikrishna Valluri, Guillermo R. Labadie, Rama Mohan Hindupur, Panicker Bijoy
Publikováno v:
Organic letters. 3(23)
[structure-see text] A convergent and stereoselective total synthesis of epothilone B (2) is described. The key steps are Normant reaction, Wadsworth-Emmons reaction of a methyl ketone 14 with the phosphonate reagent 7, diastereoselective aldol conde
Publikováno v:
Tetrahedron Letters. 42:7153-7154
A new, mild, and chemoselective method for the deprotection of trichloroethoxylcarbonyl and trichloroacetyl groups is described.