Zobrazeno 1 - 10
of 18
pro vyhledávání: '"V. T. RAVIKUMAR"'
Autor:
V. T. Ravikumar, Sunil K. Singh, Gaurav Shakya, Virinder S. Parmar, Ashok K. Prasad, Jyotirmoy Maity
Publikováno v:
The Journal of Organic Chemistry. 73:5629-5632
Candida antarctica lipase-B (CAL-B) immobilized on lewatite selectively acylated the primary hydroxyl group of the furanosyl nucleoside in a mixture of 1-(alpha-D-arabinofuranosyl)thymine and 1-(alpha-D-arabinopyranosyl)thymine. This selective biocat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ba32ff82ba167b53d90ec9303a7999d
https://doi.org/10.1021/jo800731u
https://doi.org/10.1021/jo800731u
Publikováno v:
Organic Process Research & Development. 4:225-231
A new process for the preparation of large amounts of thioate oligonucleotides in a quasi-classical solution condition is described. This method takes advantage of the use of poly(ethylene glycol) as a soluble, inert support during the synthesis. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d68831559aed65a8fc58632727e139be
https://doi.org/10.1021/op990096l
https://doi.org/10.1021/op990096l
Autor:
K.E. Frank, P. V. Devasthale, E.J. Gentry, V. T. Ravikumar, A. Keschavarz-Shokri, L. A. Mitscher, A Nilius, L. L. Shen, R. Shawar, W. R. Baker
Publikováno v:
Combinatorial Chemistry & High Throughput Screening. 1:89-99
A series of pure fluoroquinolone antiinfective agents was prepared by multiple parallel synthesis using a simple new apparatus. These compounds were evaluated biologically against Gram-positive and Gram-negative microorganisms and against a BCG strai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::272d367ec34c014d8683e5009f206efd
https://doi.org/10.2174/138620730102220119152303
https://doi.org/10.2174/138620730102220119152303
Autor:
V. T. Ravikumar, Z. S. Cheruvallath
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c315ab69b312a8395ad8507c8c1ad8db
https://doi.org/10.1002/chin.199643214
https://doi.org/10.1002/chin.199643214
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::258fdfcb175a7a1b3f44e396e6788d11
https://doi.org/10.1002/chin.199808214
https://doi.org/10.1002/chin.199808214
Autor:
K E, Frank, P V, Devasthale, E J, Gentry, V T, Ravikumar, A, Keschavarz-Shokri, L A, Mitscher, A, Nilius, L L, Shen, R, Shawar, W R, Baker
Publikováno v:
Combinatorial chemistryhigh throughput screening. 1(2)
A series of pure fluoroquinolone antiinfective agents was prepared by multiple parallel synthesis using a simple new apparatus. These compounds were evaluated biologically against Gram-positive and Gram-negative microorganisms and against a BCG strai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa8486b3fe1e26161adbc356b3f8adfb
https://pubmed.ncbi.nlm.nih.gov/10500768
https://pubmed.ncbi.nlm.nih.gov/10500768
Publikováno v:
Carbohydrate Polymers. 34:421
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::398417585e06f71e208d31db076e25a8
https://doi.org/10.1016/s0144-8617(97)87334-1
https://doi.org/10.1016/s0144-8617(97)87334-1
Publikováno v:
Tetrahedron. 44:1603-1607
Hypervalent iodine oxidation of β-diketones and β-ketoesters with iodosobenzene-boron trifluoride etherate in chloroform using appropriate nucleophiles results In α-functionalization. Benzoylacetone on reaction with iodosobenzene or iodosobenzene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c526cfe28978eff3494d08757f2b693b
https://doi.org/10.1016/s0040-4020(01)86720-x
https://doi.org/10.1016/s0040-4020(01)86720-x
Publikováno v:
The Journal of Organic Chemistry. 50:5867-5869
Synthese par addition de Michael entre la cyclopentene-1'yl-1 pyrrolidine et le (methyl-2 α-methylene) dioxolanne-1,3 propionate-2 d'ethyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1059570805555e3c18d4d9c1f66c71b1
https://doi.org/10.1021/jo00350a086
https://doi.org/10.1021/jo00350a086
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55d4290646c0335b0559f75ce6b793ff
https://doi.org/10.1002/chin.198617179
https://doi.org/10.1002/chin.198617179