Zobrazeno 1 - 3
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pro vyhledávání: '"Amanda Ramdular"'
Autor:
Amanda Ramdular, K. A. Woerpel
Publikováno v:
Org Lett
Substitution reactions of acyclic β-alkoxy acetals proceeded with generally high diastereoselectivities (>90:10) to form the anti product. Mechanistic experiments supplemented with computational studies suggest that, upon activation of the acetal, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15406792ca47dd984253c6e3e95daeb7
https://europepmc.org/articles/PMC9817112/
https://europepmc.org/articles/PMC9817112/
Autor:
Patricia Gonzalez Periche, Amanda Ramdular, Naga V.S.D.K. Bhupathiraju, Teja Kalidindi, Delissa S. Johnson, Nagavarakishore Pillarsetty, David R. Mootoo
Publikováno v:
SSRN Electronic Journal.
The THF containing acetogenin 4-deoxyannonmontacin (4-DAN) has attracted interest for its potent cytotoxicity against a broad range of human tumor cell lines, and relatively simple structure. Herein is described the synthesis and cytotoxicity of C-10
Autor:
Amanda Ramdular, K. A. Woerpel
Publikováno v:
Org Lett
Neighboring-group participation of an ester enabled stereocontrol in substitution reactions of acyclic acetals. The ester group formed a trans-fused dioxolenium ion intermediate, which underwent a substitution reaction at the acetal carbon atom to af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1192cad17f57d5a6c9e6fd147e067399
https://europepmc.org/articles/PMC7337985/
https://europepmc.org/articles/PMC7337985/