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Enantioselective Iodolactonization of Disubstituted Olefinic Acids Using a Bifunctional Catalyst

[Image: see text] The enantioselective iodolactonizations of a series of diversely-substituted olefinic carboxylic acids are promoted by a BINOL-derived, bifunctional catalyst. Reactions involving 5-alkyl- and 5-aryl-4(Z)-pentenoic acids and 6-alkyl- and 6-aryl-5(Z)-hexenoic acids provide the corres...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Fang, Chao, Paull, Daniel H., Hethcox, J. Caleb, Shugrue, Christopher R., Martin, Stephen F.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2012
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3528805/
https://ncbi.nlm.nih.gov/pubmed/23199100
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol3030555
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