Stereoselective synthesis of 2,6-cis-tetrahydropyrans through a tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect: synthesis of (+)-neopeltolide macrolactone.
Publication
, Journal Article
Kim, H; Park, Y; Hong, J
Published in: Angewandte Chemie (International ed. in English)
January 2009
Duke Scholars
Published In
Angewandte Chemie (International ed. in English)
DOI
EISSN
1521-3773
ISSN
1433-7851
Publication Date
January 2009
Volume
48
Issue
41
Start / End Page
7577 / 7581
Related Subject Headings
- Stereoisomerism
- Pyrans
- Oxidation-Reduction
- Organic Chemistry
- Molecular Structure
- Macrolides
- Lactones
- 34 Chemical sciences
- 03 Chemical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Kim, H., Park, Y., & Hong, J. (2009). Stereoselective synthesis of 2,6-cis-tetrahydropyrans through a tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect: synthesis of (+)-neopeltolide macrolactone. Angewandte Chemie (International Ed. in English), 48(41), 7577–7581. https://doi.org/10.1002/anie.200903690
Kim, Hyoungsu, Yongho Park, and Jiyong Hong. “Stereoselective synthesis of 2,6-cis-tetrahydropyrans through a tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect: synthesis of (+)-neopeltolide macrolactone.” Angewandte Chemie (International Ed. in English) 48, no. 41 (January 2009): 7577–81. https://doi.org/10.1002/anie.200903690.
Kim H, Park Y, Hong J. Stereoselective synthesis of 2,6-cis-tetrahydropyrans through a tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect: synthesis of (+)-neopeltolide macrolactone. Angewandte Chemie (International ed in English). 2009 Jan;48(41):7577–81.
Kim, Hyoungsu, et al. “Stereoselective synthesis of 2,6-cis-tetrahydropyrans through a tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect: synthesis of (+)-neopeltolide macrolactone.” Angewandte Chemie (International Ed. in English), vol. 48, no. 41, Jan. 2009, pp. 7577–81. Epmc, doi:10.1002/anie.200903690.
Kim H, Park Y, Hong J. Stereoselective synthesis of 2,6-cis-tetrahydropyrans through a tandem allylic oxidation/oxa-Michael reaction promoted by the gem-disubstituent effect: synthesis of (+)-neopeltolide macrolactone. Angewandte Chemie (International ed in English). 2009 Jan;48(41):7577–7581.
Published In
Angewandte Chemie (International ed. in English)
DOI
EISSN
1521-3773
ISSN
1433-7851
Publication Date
January 2009
Volume
48
Issue
41
Start / End Page
7577 / 7581
Related Subject Headings
- Stereoisomerism
- Pyrans
- Oxidation-Reduction
- Organic Chemistry
- Molecular Structure
- Macrolides
- Lactones
- 34 Chemical sciences
- 03 Chemical Sciences