Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Subhomoy Das"'
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 17562-17572 (2018)
Externí odkaz:
https://doaj.org/article/e2619c74485148f581b9f1402d739ccc
Publikováno v:
RSC Advances. 13:1580-1586
Chiral polymeric particles (CPPs) were studied extensively in recent years due to their importance in pharmaceutical applications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bc0f3951a0d8fa4ecffb9306f46376b
https://doi.org/10.1039/d2ra07244k
https://doi.org/10.1039/d2ra07244k
Publikováno v:
Nature Physics. 18:1177-1180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f1c932d4702f5b54b26bb4ad43cbccf
https://doi.org/10.1038/s41567-022-01705-w
https://doi.org/10.1038/s41567-022-01705-w
Autor:
Subhomoy Das, Koena Ghosh
Publikováno v:
Organic & Biomolecular Chemistry. 19:965-982
Ring-opening transformations of donor-acceptor cyclopropanes (DAC) with carbon-centered nucleophiles is a simple, straight-forward approach to 1,3-bifunctional compounds that has witnessed remarkable progress over the past several years. To date, dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78fe2cf1b9b4c5493ca3957186db03a0
https://doi.org/10.1039/d0ob02437f
https://doi.org/10.1039/d0ob02437f
Publikováno v:
Synlett. 31:708-712
A simple strategy to access a wide range of substituted oxime amino ethers in good to high yields via Lewis acid catalyzed SN2-type ring opening of activated aziridines with aryl aldehyde oximes is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04c6afc27ebeb858bc719f20e86a5714
https://doi.org/10.1055/s-0039-1691596
https://doi.org/10.1055/s-0039-1691596
Publikováno v:
The Journal of Organic Chemistry. 85:367-379
A mild one-pot stereospecific synthetic route to highly functionalized imidazolidines and oxazolidines via SN2-type ring-opening of the corresponding activated aziridines and epoxides with amines followed by p-toluenesulfonic acid (PTSA)-catalyzed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1818c0e0fc12cee3189ad00a42a6c2
https://doi.org/10.1021/acs.joc.9b02278
https://doi.org/10.1021/acs.joc.9b02278
Publikováno v:
New Journal of Chemistry. 43:1993-2001
We report the significant rate enhancement of the Mizoroki–Heck reaction by in situ generated palladium nanoclusters within the confined space of water-in-oil (w/o) mixed microemulsion (μE) formulated by sodium dodecylsulfate (SDS), polyoxyethylen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a57549e5d82665f669813bc11d83a79
https://doi.org/10.1039/c8nj05118f
https://doi.org/10.1039/c8nj05118f
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 17562-17572 (2018)
A simple synthetic route to access racemic 3,3-disubstituted propylamines in excellent yields (up to 95%) via Lewis acid catalyzed SN2-type ring opening of activated azetidines with electron-rich a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18ebbbb12f581ffee10974cfd51f9123
https://doaj.org/article/e2619c74485148f581b9f1402d739ccc
https://doaj.org/article/e2619c74485148f581b9f1402d739ccc
Publikováno v:
The Journal of Organic Chemistry. 83:14553-14567
A highly efficient and stereoselective route to access 1,3-disubstituted 1,2,3,4-tetrahydropyrazino[1,2-a]indoles and 3,4-dihydro-1H-[1,4]oxazino[4,3-a]indoles with excellent stereoselectivity (de, ee >99%) via base mediated ring opening of aziridine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc82f2c5d03a16e1ba07d466de22fe3
https://doi.org/10.1021/acs.joc.8b02339
https://doi.org/10.1021/acs.joc.8b02339
Publikováno v:
Tetrahedron. 93:132285
Enolate mediated domino imino-aldol-aza-Michael and domino imino-aldol-aza-Michael-imino-aldol reactions of α-(aryl/alkyl)methylidene-β-diketones with activated N-aryl aldimines (1.0 and 2.0 equiv., respectively) have been developed for the diaster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc51bb8a993827af9341043e9cc5d089
https://doi.org/10.1016/j.tet.2021.132285
https://doi.org/10.1016/j.tet.2021.132285