Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Elizabeth C. Dugan"'
Autor:
Marisa C. Kozlowski, Evan S. DiVirgilio, Elizabeth C. Dugan, Gerhard Bringmann, Katja Maksimenka
Publikováno v:
Advanced Synthesis & Catalysis. 349:583-594
An enantioselective synthesis of the chiral bisnaphthopyrone natural product nigerone and its enantiomer, ent-nigerone, has been realized. The use of constrained 2-naphthol substrates was critical to producing highly functionalized chiral 1,1′-bina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::459f40d4a4fa71df3ff60a4886dce6dd
https://doi.org/10.1002/adsc.200600570
https://doi.org/10.1002/adsc.200600570
Publikováno v:
Organic Letters. 9:385-388
[reaction: see text] An enantioselective synthesis of the chiral bisnaphthopyrone natural product nigerone is reported. The key step was an eight-step isomerization process to form the final natural product. The isomerization precursor was constructe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d57200e563722e31ca9dcdbb09630be
https://doi.org/10.1021/ol062468y
https://doi.org/10.1021/ol062468y
Autor:
Thomas D. Clark, Elizabeth C. Dugan
Publikováno v:
Synthesis. :1083-1086
This paper describes the synthesis of hexa(ethylene glycol) and carboxymethylhexa(ethylene glycol)-terminated alkane-disulfides 4 and 7, respectively, in which the alkylene chains are twenty-methylenes-long. The key twenty-carbon synthon, 20-bromoico
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e23d47f1134f0bb3f69c4f4d41d7cbcc
https://doi.org/10.1055/s-2006-926377
https://doi.org/10.1055/s-2006-926377