Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sudhindra H. Deshpande"'
Autor:
Jagadeesh P. Kilaru, Ravindra Sonawane, Sitaram Pal, Mark Montgomery, Vanitha Acharya, Sudhindra H. Deshpande, Sanjib Mal, Bhanu N. Manjunath
Publikováno v:
European Journal of Organic Chemistry. 2020:378-387
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea9448e7ab304369a120531adb3d7ee4
https://doi.org/10.1002/ejoc.201901649
https://doi.org/10.1002/ejoc.201901649
Publikováno v:
Synthesis. 49:2435-2442
A simple, fast and efficient synthesis of 3-phosphorylated benzoxaboroles using the Pudovik reaction is reported. A number of diverse 3-(dialkoxyphosphoryl)-1-hydroxy-3H-2,1-benzoxaboroles were synthesised in 70–86% yield. Interesting hydrogen bond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30648af7b7ae071b806af8b3b27595e0
https://doi.org/10.1055/s-0036-1588739
https://doi.org/10.1055/s-0036-1588739
Publikováno v:
ChemistrySelect. 1:2221-2224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0dc31cc91fc1090a70aaad51e3dc286
https://doi.org/10.1002/slct.201600497
https://doi.org/10.1002/slct.201600497
Autor:
Vedavati G. Puranik, Ashutosh A. Kelkar, Savita Kiran Shingote, Debamitra Chakravarty, Raghunath V. Chaudhari, Sudhindra H. Deshpande, Vaishali S. Shende
Publikováno v:
RSC Advances. 5:51722-51729
New unsymmetrical vicinal diamine ligands with systematic variation in the regio and stereo positions in the amine and sulphonamide groups were synthesized from cheap starting material such as norephedrine. Catalytic Asymmetric Transfer Hydrogenation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81533de035bde0a7bfe48cfcbf080ab5
https://doi.org/10.1039/c5ra08220j
https://doi.org/10.1039/c5ra08220j
Autor:
Rupesh Patre, Sanjib Mal, Bhanu N. Manjunath, Sudhindra H. Deshpande, Pankaj R. Nilkanth, Sitaram Pal, Sujit K. Ghorai, Tomas Smejkal, Myriem El Qacemi
Publikováno v:
Chemical communications (Cambridge, England). 53(15)
A bio-catalyzed N-formylation reaction of different amines has been developed using ethyl formate as a formylating agent. This protocol provides a facile and convenient strategy featuring mild reaction conditions, high efficacy, a broad substrate sco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92ef2ac69da8d6db429cbd358ab8b944
https://pubmed.ncbi.nlm.nih.gov/28174765
https://pubmed.ncbi.nlm.nih.gov/28174765
Autor:
Kumar Vanka, Savita Kiran Shingote, Ashutosh Anant Kelkar, Vaishali S. Shende, Sudhindra H. Deshpande, Nishamol Kuriakose
Publikováno v:
RSC Adv.. 4:46351-46356
Asymmetric transfer hydrogenation of various cyclic imines proceeded efficiently with water/methanol co-solvent media in 20 min with excellent yields and enantioselectivities by employing Rh–TsDPEN catalyst and sodium formate as a hydrogen donor. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60275537917c80400645687ff7f205e9
https://doi.org/10.1039/c4ra07964g
https://doi.org/10.1039/c4ra07964g
Autor:
Rajesh G. Gonnade, Savita Kiran Shingote, Sudhindra H. Deshpande, Ashutosh A. Kelkar, Raghunath V. Chaudhari
Publikováno v:
Catalysis Letters. 138:231-238
Catalytic asymmetric transfer hydrogenation of aromatic alkyl ketones has been investigated using [Ru(p-cymene)Cl2]2 and new derivatives of β-amino alcohols synthesized from (S)-(−)-lactic acid and mandelic acid as ligands. Chiral secondary alcoho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b178029d4d92ecf59487e87c52ed1c19
https://doi.org/10.1007/s10562-010-0408-y
https://doi.org/10.1007/s10562-010-0408-y
Autor:
Ashutosh A. Kelkar, Anu Joseph, Sudhindra H. Deshpande, Savita Kiran Shingote, Vaishali S. Shende
Publikováno v:
Organic letters. 17(12)
Asymmetric transfer hydrogenation (ATH) of imines has been performed with variation in formic acid (F) and triethylamine (T) molar ratios in water. The F/T ratio is shown to affect both the reduction rate and enantioselectivity, with the optimum rati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38ca0cfff701efe5784644b7af3a5541
https://pubmed.ncbi.nlm.nih.gov/26023885
https://pubmed.ncbi.nlm.nih.gov/26023885
Autor:
Kumar Vanka, Nishamol Kuriakose, Sudhindra H. Deshpande, Ashutosh Anant Kelkar, Vaishali S. Shende, Savita Kiran Shingote
Publikováno v:
ChemInform. 46
1-Substituted 6,7-dimethoxy-3,4-dihydroisoquinolines (I) and (III) are used as substrates in the title reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41ae1cf853cb8164e344c995eaccb6d1
https://doi.org/10.1002/chin.201514203
https://doi.org/10.1002/chin.201514203