Total synthesis of cyanolide A and confirmation of its absolute configuration.
Publication
, Journal Article
Kim, H; Hong, J
Published in: Organic letters
June 2010
The tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect and the 2-methyl-6-nitrobenzoic anhydride (MNBA)-mediated dimerization were explored for the efficient and facile synthesis of cyanolide A.
Duke Scholars
Published In
Organic letters
DOI
EISSN
1523-7052
ISSN
1523-7060
Publication Date
June 2010
Volume
12
Issue
12
Start / End Page
2880 / 2883
Related Subject Headings
- Schistosoma
- Oxidation-Reduction
- Organic Chemistry
- Nitrobenzoates
- Molecular Structure
- Macrolides
- Glycosylation
- Animals
- Anhydrides
- 34 Chemical sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Kim, H., & Hong, J. (2010). Total synthesis of cyanolide A and confirmation of its absolute configuration. Organic Letters, 12(12), 2880–2883. https://doi.org/10.1021/ol101022z
Kim, Hyoungsu, and Jiyong Hong. “Total synthesis of cyanolide A and confirmation of its absolute configuration.” Organic Letters 12, no. 12 (June 2010): 2880–83. https://doi.org/10.1021/ol101022z.
Kim H, Hong J. Total synthesis of cyanolide A and confirmation of its absolute configuration. Organic letters. 2010 Jun;12(12):2880–3.
Kim, Hyoungsu, and Jiyong Hong. “Total synthesis of cyanolide A and confirmation of its absolute configuration.” Organic Letters, vol. 12, no. 12, June 2010, pp. 2880–83. Epmc, doi:10.1021/ol101022z.
Kim H, Hong J. Total synthesis of cyanolide A and confirmation of its absolute configuration. Organic letters. 2010 Jun;12(12):2880–2883.
Published In
Organic letters
DOI
EISSN
1523-7052
ISSN
1523-7060
Publication Date
June 2010
Volume
12
Issue
12
Start / End Page
2880 / 2883
Related Subject Headings
- Schistosoma
- Oxidation-Reduction
- Organic Chemistry
- Nitrobenzoates
- Molecular Structure
- Macrolides
- Glycosylation
- Animals
- Anhydrides
- 34 Chemical sciences