Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Uredi Dilipkumar"'
Autor:
Burra, Amarender G.1 (AUTHOR), Uredi, Dilipkumar1 (AUTHOR), Motati, Damoder R.1 (AUTHOR), Fronczek, Frank R.2 (AUTHOR), Watkins, E. Blake1 (AUTHOR) bwatkins@uu.edu
Publikováno v:
European Journal of Organic Chemistry. 8/26/2022, Vol. 2022 Issue 32, p1-6. 6p.
Akademický článek
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Publikováno v:
Synthetic Communications. 49:2709-2716
A synthetic strategy for the proposed structure of the pandangolide 1 is disclosed starting from 1,3-propane diol in 18-steps. Sharpless asymmetric dihydroxylation, Keck allylation, Yamaguchi ester...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::910c511b385134b7471fb1b8f8531521
https://doi.org/10.1080/00397911.2019.1639757
https://doi.org/10.1080/00397911.2019.1639757
Publikováno v:
In Studies in Natural Products Chemistry 2019 63:81-112
Akademický článek
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Publikováno v:
Chemical Communications. 53:1904-1907
A novel one-pot benzannulation reaction has been developed for the synthesis of substituted polycyclic aromatic hydrocarbons (PAHs) from the direct coupling of propargylic aldehydes/alcohols with 1,1-diarylethanol through an atom-economical uninterru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42f57cccf2df89c7f36309d7a24c312
https://doi.org/10.1039/c6cc09108c
https://doi.org/10.1039/c6cc09108c
Publikováno v:
Journal of Organic Chemistry; 12/17/2021, Vol. 86 Issue 24, p17748-17761, 14p
A synthetic strategy for the proposed structure of the pandangolide 1 is disclosed starting from 1,3-propane diol in 18-steps. Sharpless asymmetric dihydroxylation, Keck allylation, Yamaguchi esterification, and Grubbs ring closing metathesis were th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400a31e4e3ec308a7591371fa19564cd
Publikováno v:
Tetrahedron: Asymmetry. 27:222-225
The asymmetric total synthesis of cladospolide D, a natural 12-membered macrolide antibiotic, has been accomplished in 12-steps. Sharpless asymmetric dihydroxylation, Grubb’s cross metathesis, and Shiina lactonization have been employed as the key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3c5c8bfc29a8a4e795ca216eb963b7a
https://doi.org/10.1016/j.tetasy.2016.01.013
https://doi.org/10.1016/j.tetasy.2016.01.013
Publikováno v:
Chemistry - A European Journal. 22:2501-2506
A novel one-pot [4+2]-benzannulation approach to substituted carbazoles is accomplished by acid-catalyzed C3-propargylation of 2-alkenyl/aryl indoles with 1-aryl propargylic alcohols, followed by cycloisomerization. A variety of 2-alkenylated indoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddc9f344c4e3fa7c8f8f7e69efd0e1e5
https://doi.org/10.1002/chem.201503496
https://doi.org/10.1002/chem.201503496