Zobrazeno 1 - 10
of 164
pro vyhledávání: '"Dhevalapally B. Ramachary"'
Publikováno v:
ACS Organic & Inorganic Au, Vol 4, Iss 5, Pp 534-544 (2024)
Externí odkaz:
https://doaj.org/article/0c743dade063497b8361a3faf776547a
Publikováno v:
Molecules, Vol 26, Iss 14, p 4320 (2021)
Biologically important, chiral natural products of butenolides, (−)-blastmycinolactol, (+)-blastmycinone, (−)-NFX-2, (+)-antimycinone, lipid metabolites, (+)-ancepsenolide, (+)-homoancepsenolide, mosquito larvicidal butenolide and their analogues
Externí odkaz:
https://doaj.org/article/90738a54e40d4dcebbd33c36719a54df
Publikováno v:
ACS Omega, Vol 2, Iss 10, Pp 6514-6524 (2017)
Externí odkaz:
https://doaj.org/article/db4455d2032347f1a733066bf57a6c3f
Publikováno v:
ARKIVOC, Vol 2016, Iss 2, Pp 98-115 (2015)
Externí odkaz:
https://doaj.org/article/c072ddae33ac44bb94b5c3005adac8fe
Publikováno v:
The Journal of Organic Chemistry. 87:16026-16038
Biologically important 4-alkylsyncarpic acids, which resemble the core structure of many natural products, were synthesized in one-pot through the organocatalytic three-component reductive alkylation with excellent yields and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37b2389493e2e12a0cfe3c3fe770408e
https://doi.org/10.1021/acs.joc.2c02164
https://doi.org/10.1021/acs.joc.2c02164
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3d17bbcc2716e258c0a74849092ad92
https://doi.org/10.1021/acs.joc.3c00070
https://doi.org/10.1021/acs.joc.3c00070
Publikováno v:
Organic & Biomolecular Chemistry. 20:3948-3954
3-Aryllawsones are well known for their wide range of applications in medicinal chemistry, but their synthesis has always remained challenging as no comprehensive protocol has been outlined to date. Owing to their structural importance, we synthesize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b45ae6700e131e0fddca522b7e54872
https://doi.org/10.1039/d2ob00438k
https://doi.org/10.1039/d2ob00438k
Publikováno v:
Supramolecular Catalysis. :441-449
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da6abd8a5c918fff72f80a489f694d32
https://doi.org/10.1002/9783527832033.ch30
https://doi.org/10.1002/9783527832033.ch30
Publikováno v:
Chemistry – A European Journal. 27:18033-18038
3-Alkyl-lawsones selectively reacted with α-alkyl-nitroethylenes under 500 parts-per-million (ppm) quinine-NH-thiourea-catalysis to furnish the chiral methanobenzo[7]annulenes in up to >99 % ee with >20 : 1 dr and TON up to 1820 through tandem Micha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b8defe12a56c19ca3b7485883a73666
https://doi.org/10.1002/chem.202103254
https://doi.org/10.1002/chem.202103254
Autor:
Swamy Peraka, Badaraita Gorachand, Akram Hussain, Revoju Sravanthi, Dhevalapally B. Ramachary
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56da1cf024f930d902c8ca9bfc73efa1
https://doi.org/10.1002/ejoc.202201133
https://doi.org/10.1002/ejoc.202201133