Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Supriya, Ghanty"'
Publikováno v:
The Journal of organic chemistry. 87(1)
A novel methodology for the arylation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93ab6772d1d8ff030b7f2ddec013ba88
https://pubmed.ncbi.nlm.nih.gov/34958570
https://pubmed.ncbi.nlm.nih.gov/34958570
Publikováno v:
Tetrahedron: Asymmetry. 26:885-890
The asymmetric total synthesis of marine polypropionate natural products siphonarienal and siphonarienone has been achieved from a common precursor 3 . The key transformations of this synthesis are the diastereoselective oxidative kinetic resolution,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b251950d6cb42d5da2b370b46fa86701
https://doi.org/10.1016/j.tetasy.2015.07.001
https://doi.org/10.1016/j.tetasy.2015.07.001
Publikováno v:
Tetrahedron Letters. 55:4298-4301
The coupling of aldehydes or ketones with (2-(4-methoxyphenyl)-4-methylenetetrahydrofuran-3-yl)methanol in the presence of nitriles under the influence of 5 mol % tris(pentaflourophenyl)borane at room temperature afforded a novel series of cis-fused
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14087699009a3557fbe26c590ef58733
https://doi.org/10.1016/j.tetlet.2014.05.115
https://doi.org/10.1016/j.tetlet.2014.05.115
Autor:
Supriya Ghanty, B. V. Subba Reddy
Publikováno v:
ChemInform. 46
A highly diastereoselective synthesis of the title compounds is achieved using a o-benzenedisulfonimide as catalyst under mild conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::139f8389b30962ca9ef93c2ae75504ec
https://doi.org/10.1002/chin.201501160
https://doi.org/10.1002/chin.201501160
Publikováno v:
ChemInform. 46
A facile protocol is developed for the three component reaction of tetrahydrofuran substrates (I) with carbonyl compounds and nitriles to produce the title compounds (IV), (VI), and (IX) under mild conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e623236a3f6af9b51ed0601674124e0
https://doi.org/10.1002/chin.201502135
https://doi.org/10.1002/chin.201502135
A stereoselective total synthesis of the 2-(2-hydroxyalkyl)piperidine alkaloids has been accomplished by a Prins–Ritter amidation sequence. Other steps involved in this synthesis are Jacobsen's hydrolytic kinetic resolution (HRK) and ring-closing m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::399675c9e8c4fee373b20da3c536b194
Autor:
Supriya Ghanty, B. V. Subba Reddy
A highly diastereoselective synthesis of 4-amidotetrahydropyran derivatives has been achieved using a catalytic amount of o-benzenedisulfonimide under mild conditions involving sequential allylation and Prins–Ritter amidation. The oxo-carbenium ion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62e976d63bd6b84d85916f150a4466f4