A stereoselective formal synthesis of leucascandrolide A.
Publication
, Journal Article
Lee, K; Kim, H; Hong, J
Published in: Organic letters
May 2011
A stereoselective formal synthesis of leucascandrolide A was accomplished through the tandem and organocatalytic oxa-Michael reactions, which were promoted by the gem-disubstituent effect, in conjunction with the dithiane coupling reaction.
Duke Scholars
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Published In
Organic letters
DOI
EISSN
1523-7052
ISSN
1523-7060
Publication Date
May 2011
Volume
13
Issue
10
Start / End Page
2722 / 2725
Related Subject Headings
- Sulfur Compounds
- Stereoisomerism
- Sesquiterpenes
- Quinolizines
- Porifera
- Organic Chemistry
- Molecular Structure
- Catalysis
- Animals
- 34 Chemical sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Lee, K., Kim, H., & Hong, J. (2011). A stereoselective formal synthesis of leucascandrolide A. Organic Letters, 13(10), 2722–2725. https://doi.org/10.1021/ol200824r
Lee, Kiyoun, Hyoungsu Kim, and Jiyong Hong. “A stereoselective formal synthesis of leucascandrolide A.” Organic Letters 13, no. 10 (May 2011): 2722–25. https://doi.org/10.1021/ol200824r.
Lee K, Kim H, Hong J. A stereoselective formal synthesis of leucascandrolide A. Organic letters. 2011 May;13(10):2722–5.
Lee, Kiyoun, et al. “A stereoselective formal synthesis of leucascandrolide A.” Organic Letters, vol. 13, no. 10, May 2011, pp. 2722–25. Epmc, doi:10.1021/ol200824r.
Lee K, Kim H, Hong J. A stereoselective formal synthesis of leucascandrolide A. Organic letters. 2011 May;13(10):2722–2725.
Published In
Organic letters
DOI
EISSN
1523-7052
ISSN
1523-7060
Publication Date
May 2011
Volume
13
Issue
10
Start / End Page
2722 / 2725
Related Subject Headings
- Sulfur Compounds
- Stereoisomerism
- Sesquiterpenes
- Quinolizines
- Porifera
- Organic Chemistry
- Molecular Structure
- Catalysis
- Animals
- 34 Chemical sciences