Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Sudhakar R. Bhusare"'
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 2091-2097 (2019)
A new series of pyrazole, isoxazole, benzoxazepine, benzothiazepine and benzodiazepine derivatives were prepared by the multi-component cyclo-condensation reaction of 1-phenyl-3-(2-(tosyloxy)phenyl)propane-1,3-dione, N,N-dimethylformamide dimethyl ac
Externí odkaz:
https://doaj.org/article/58f745970a9f426caf68604c9a1e11e7
Autor:
Satish A. Dake, Sunil U. Tekale, Swapnil R. Sarda, Wamanrao N. Jadhav, Sudhakar R. Bhusare, Rajendra P. Pawar
Publikováno v:
ARKIVOC, Vol 2008, Iss 17, Pp 241-247 (2009)
Externí odkaz:
https://doaj.org/article/f8f34679923d405aa8e1ba5849cc6622
Publikováno v:
ARKIVOC, Vol 2006, Iss 1, Pp 104-108 (2005)
Externí odkaz:
https://doaj.org/article/483c09edf0f6423fb005a621807de5c4
Publikováno v:
American Journal of PharmTech Research. 10:55-73
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20d3135e0b2a690c025bce1169559fee
https://doi.org/10.46624/ajptr.2020.v10.i1.006
https://doi.org/10.46624/ajptr.2020.v10.i1.006
Autor:
Wamanrao N. Jadhav, Santosh V. Goswami, Shrikant S. Pendalwar, Sudhakar R. Bhusare, Madhavi S. Menkudle
Publikováno v:
SN Applied Sciences. 2
An asymmetric Baylis–Hillman reaction protocol has been developed using a chiral pyrrolidine based organocatalyst. The catalytic loading works well with a wide range of aromatic aldehydes to afford the corresponding β-hydroxy acrylate with high en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::790269ce213ba7306a47cdd8d6d90d42
https://doi.org/10.1007/s42452-020-2507-8
https://doi.org/10.1007/s42452-020-2507-8
Autor:
Hanmant M. Kasralikar, Shivaji B. Patwari, Sudhakar R. Bhusare, Sujit G. Bhansali, Suresh C. Jadhavar
Publikováno v:
Journal of Heterocyclic Chemistry. 55:821-829
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b0fb863d3e3dc1a9e04e29be704debd
https://doi.org/10.1002/jhet.3103
https://doi.org/10.1002/jhet.3103
Publikováno v:
Asian Journal of Green Chemistry, Vol 3, Iss Issue 2. pp. 125-287, Pp 201-215 (2019)
Novel two L-proline analogues as thiourea organocatalysts were synthesised, first is the assembly of a structurally well-defined cyclohexane scaffold with a thiourea moieties and amine functionalities could constitute a new class of organocatalysts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::888b41a02c16b08b9ff1c869c19bce58
https://doi.org/10.14233/ajomc.2018.ajomc-p132
https://doi.org/10.14233/ajomc.2018.ajomc-p132
Publikováno v:
Research on Chemical Intermediates. 43:7211-7221
A green protocol for an effective synthesis of bioactive polyhydroquinoline derivatives was developed via condensation of substituted salicylaldehyde, dimedone, ethyl acetoacetate and ammonium acetate catalyzed by 3-methyl-1-sulfonic acid imidazolium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cebe1a9e3d4c3eb4fc4143dd320cb330
https://doi.org/10.1007/s11164-017-3069-2
https://doi.org/10.1007/s11164-017-3069-2
Publikováno v:
Chinese Chemical Letters. 29:942-944
The proline based chiral organocatalyst has been found to be an efficient catalyst for the facile synthesis of substituted 2-aryl-2H-chromenes-3-carbaldehyde. We envisioned that the iminium interaction between chiral amino catalysts and α,β-unsatur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::891da16c815b139465bd6bc54e4215d7
https://doi.org/10.1016/j.cclet.2017.09.058
https://doi.org/10.1016/j.cclet.2017.09.058
Publikováno v:
Synlett. 26:1969-1972
l -Proline has been employed efficiently for the synthesis of chromeno-chromenone derivatives via a one-pot, three component condensation reaction of salicylaldehydes, 4-hydroxy coumarin, and indole or barbituric acid. The simple procedure and good t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::353950b82294b91a3b25c609259c687b
https://doi.org/10.1055/s-0034-1381043
https://doi.org/10.1055/s-0034-1381043