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A formal synthesis of SCH 351448.

Publication ,  Journal Article
Park, H; Kim, H; Hong, J
Published in: Organic letters
July 2011

An efficient formal synthesis of SCH 351448 was accomplished through the tandem cross-metathesis (CM)/oxa-Michael, the 1,4-syn aldol, the tandem oxidation/oxa-Michael, and the Suzuki coupling reaction.

Duke Scholars

Published In

Organic letters

DOI

EISSN

1523-7052

ISSN

1523-7060

Publication Date

July 2011

Volume

13

Issue

14

Start / End Page

3742 / 3745

Related Subject Headings

  • Stereoisomerism
  • Oxidation-Reduction
  • Organic Chemistry
  • Molecular Structure
  • Lactones
  • Aldehydes
  • 34 Chemical sciences
  • 03 Chemical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Park, H., Kim, H., & Hong, J. (2011). A formal synthesis of SCH 351448. Organic Letters, 13(14), 3742–3745. https://doi.org/10.1021/ol201426c
Park, Heekwang, Hyoungsu Kim, and Jiyong Hong. “A formal synthesis of SCH 351448.Organic Letters 13, no. 14 (July 2011): 3742–45. https://doi.org/10.1021/ol201426c.
Park H, Kim H, Hong J. A formal synthesis of SCH 351448. Organic letters. 2011 Jul;13(14):3742–5.
Park, Heekwang, et al. “A formal synthesis of SCH 351448.Organic Letters, vol. 13, no. 14, July 2011, pp. 3742–45. Epmc, doi:10.1021/ol201426c.
Park H, Kim H, Hong J. A formal synthesis of SCH 351448. Organic letters. 2011 Jul;13(14):3742–3745.
Journal cover image

Published In

Organic letters

DOI

EISSN

1523-7052

ISSN

1523-7060

Publication Date

July 2011

Volume

13

Issue

14

Start / End Page

3742 / 3745

Related Subject Headings

  • Stereoisomerism
  • Oxidation-Reduction
  • Organic Chemistry
  • Molecular Structure
  • Lactones
  • Aldehydes
  • 34 Chemical sciences
  • 03 Chemical Sciences