Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nantachai Inprung"'
Autor:
Punlop Kuntiyong, Nantachai Inprung, Sineenart Attanonchai, Wichita Kheakwanwong, Pijitra Bunrod, Sunisa Akkarasamiyo
Publikováno v:
Synlett. 33:1377-1382
8-Aminoindolizidines were synthesized from l-asparagine as the chiral starting material. The key dibenzylamino succinimide intermediate was synthesized in two steps. Three homologs of chiral hydroxy lactams tethered with hydroxyalkenes were synthesiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdbbb1bb82f9b0b5e69c60de9ce719b2
https://doi.org/10.1055/a-1806-6089
https://doi.org/10.1055/a-1806-6089
Autor:
Nantachai Inprung, Hon Eong Ho, James A. Rossi-Ashton, Ryan G. Epton, Adrian C. Whitwood, Jason M. Lynam, Richard J. K. Taylor, Michael J. James, William P. Unsworth
Publikováno v:
Organic Letters. 24:668-674
Indole-ynones have been established as general substrates for radical dearomatizing spirocyclization cascade reactions. Five distinct and varied synthetic protocols have been developed─cyanomethylation, sulfonylation, trifluoromethylation, stannyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3217e7dca5f5085e4e5f9eddc1fd622e
https://doi.org/10.1021/acs.orglett.1c04098
https://doi.org/10.1021/acs.orglett.1c04098
Publikováno v:
Organic Letters
An operationally simple, high yielding three-step cascade process is described for the direct conversion of indole-tethered ynones into functionalized quinolines. A single "multitasking" thiol reagent is used to promote a three-step dearomatizing spi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c675db7754da999dcf7ff6acacb487
https://eprints.whiterose.ac.uk/171748/1/Mon_cascade_paper_version_18_revision.pdf
https://eprints.whiterose.ac.uk/171748/1/Mon_cascade_paper_version_18_revision.pdf
Autor:
Duangkamon Namborisut, Chanumas Sae-guay, Suchanart Thongteerapab, Punlop Kuntiyong, Jeeranan Sathongjin, Pijitra Bunrod, Pakaporn Khemthong, Nantachai Inprung
Publikováno v:
Tetrahedron. 73:4426-4432
Both enantiomers of C10b methyl analogs of crispine A and a tetracyclic core of Erythrina alkaloids were synthesized starting from l -aspartic acid via a common chiral N -arylethyl succinimide intermediate. The pivotal C10a-C10b bond formation and co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c18df4e31cc07c588580b919ad25388b
https://doi.org/10.1016/j.tet.2017.06.007
https://doi.org/10.1016/j.tet.2017.06.007
Autor:
Artid Buaphan, Kunita Phakdeeyothin, Punlop Kuntiyong, Nantachai Inprung, Kittisak Thammapichai
Publikováno v:
Tetrahedron. 76:131261
Spiro[indolizidine-1,3′-oxindole] compounds have been synthesized in enantiomerically pure form from l -glutamic acid. The key oxidative ring contraction of chiral indolo[2,3-a]quinolizidinone was achieved by treatment with N-bromosuccinimide in te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44ec7f5530abcb49bc5ccdb5bc92f138
https://doi.org/10.1016/j.tet.2020.131261
https://doi.org/10.1016/j.tet.2020.131261