Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Dinesh S. Bhalerao"'
Publikováno v:
ARKIVOC, Vol 2010, Iss 2, Pp 118-126 (2010)
Externí odkaz:
https://doaj.org/article/5577b877171348e493adf8d450092991
Autor:
Anil Kumar Reddy Arkala, Dinesh S. Bhalerao, Srinivas Reddy Gade, Rakeshwar Bandichhor, M. Nagaraju, Vilas Hareshwar Dahanukar, U. K. Syam Kumar, Y. V. Madhavi
Publikováno v:
Organic Process Research & Development. 19:1559-1567
Efforts toward the synthesis and process optimization of boceprevir 1 are described. Boceprevir synthesis was optimized by telescoping the first three steps and last two steps of the five-step process. Optimization of oxidation, which is one of the c
Autor:
Dinesh S. Bhalerao, Unniaran K. Syam Kumar, Shyamapada Banerjee, Satish P. Nikumbh, Rajeshwar Reddy Govindapur, Srinivasan Kaliyaperumal Appaye
Publikováno v:
Helvetica Chimica Acta. 97:1115-1122
A simple and efficient metal-free ethenolate transfer reaction has been elaborated in moderate-to-high yields from vinyl acetate. This reaction was accomplished by generation of potassium ethenolate, which was then reacted with homo and mixed anhydri
Autor:
Rakeshwar Bandichhor, Dinesh S. Bhalerao, G. C. M. Kondaiah, Padi Pratap Reddy, Arnab Roy, Apurba Bhattacharya, Lakkala Amarnath Reddy, Gudimalla Nagaraju, Ravi Kumar Mylavarappu, Namrata Dwivedi
Publikováno v:
Synthetic Communications. 40:2983-2987
A novel approach for the synthesis of omeprazole, a potent antiulcer drug, is described. The synthetic procedure involved the formation of an ester of the 5-methoxy thiobenzimidazole followed by coupling of the ester with the Grignard reagent of 2-ch
Publikováno v:
ARKIVOC, Vol 2010, Iss 2, Pp 118-126 (2010)
Biologically important process of oxidation of amidoximes has been investigated using IBX (o- iodoxybenzoic acid) and combination of IBX with TEAB (tetraethylammonium bromide). The reaction proceeds with high % conversion leading to selective formati
Publikováno v:
Synthetic Communications. 40:799-807
An efficient and convenient method for α-thiocyanation of ketones and β-dicarbonyl compounds has been developed using a reagent combination of bromodimethylsulfonium bromide (BDMS) and ammonium thiocyanate in acetonitrile. The developed method is m
Autor:
Abhijeet Kumar, Arnab Roy, Apurba Bhattacharya, Saurya Chakraborty, Jyothirmayi Naram, Lekkala Amarnath Reddy, Dinesh S. Bhalerao, Rodda Swapna, Rakeshwar Bandichhor, Bangaru Babu, Vurimidi Himabindu, M. Ravikumar, Golla China Malakondaiah, Gade Srinivas Reddy, Namrata Dwivedi
Publikováno v:
Organic Process Research & Development. 14:362-368
Efforts toward the synthesis and process optimization of amtolmetin guacil 1 are described. High-yielding electrophilic substitution followed by Wolf−Kishner reduction are the key features in the novel synthesis of tolmetin 2 which is an advanced i
Publikováno v:
Synthetic Communications. 38:2814-2819
A mild and selective procedure for the bromination of activated arenes using o-iodoxybenzoic acid and tetraethylammonium bromide is presented. The reactions were carried out at room temperature and gave moderate to excellent yields.
Publikováno v:
Synlett. 2007:2952-2956
Various aromatic and heteroaromatic compounds have been efficiently thiocyanated by using a novel combination ofbromodimethylsulfonium bromide (BDMS) and ammonium thiocyanate.
Publikováno v:
Synlett. 2007:2815-2818
Novel and facile transformation of N,N-disubstituted glycylamides into corresponding cyanamides using pentavalent -iodine reagents and tetraethylammonium bromide is discussed. The advantages of this system are use of non toxic reagents, shorter -reac