Total synthesis of d,1-occidentalol by photoannelation
Publication
, Journal Article
Baldwin, SW; Landmesser, NG
Published in: Tetrahedron Letters
January 1, 1982
A nine step synthesis of an intermediate previously used in the synthesis of the sesquiterpene occidentalol is reported which incorporates a 2+2 photocycloaddition reaction as the key carbon carbon bond forming step. © 1982.
Duke Scholars
Published In
Tetrahedron Letters
DOI
ISSN
0040-4039
Publication Date
January 1, 1982
Volume
23
Issue
43
Start / End Page
4443 / 4446
Related Subject Headings
- Organic Chemistry
- 3405 Organic chemistry
- 3404 Medicinal and biomolecular chemistry
- 3101 Biochemistry and cell biology
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry
Citation
APA
Chicago
ICMJE
MLA
NLM
Baldwin, S. W., & Landmesser, N. G. (1982). Total synthesis of d,1-occidentalol by photoannelation. Tetrahedron Letters, 23(43), 4443–4446. https://doi.org/10.1016/S0040-4039(00)85623-3
Baldwin, S. W., and N. G. Landmesser. “Total synthesis of d,1-occidentalol by photoannelation.” Tetrahedron Letters 23, no. 43 (January 1, 1982): 4443–46. https://doi.org/10.1016/S0040-4039(00)85623-3.
Baldwin SW, Landmesser NG. Total synthesis of d,1-occidentalol by photoannelation. Tetrahedron Letters. 1982 Jan 1;23(43):4443–6.
Baldwin, S. W., and N. G. Landmesser. “Total synthesis of d,1-occidentalol by photoannelation.” Tetrahedron Letters, vol. 23, no. 43, Jan. 1982, pp. 4443–46. Scopus, doi:10.1016/S0040-4039(00)85623-3.
Baldwin SW, Landmesser NG. Total synthesis of d,1-occidentalol by photoannelation. Tetrahedron Letters. 1982 Jan 1;23(43):4443–4446.
Published In
Tetrahedron Letters
DOI
ISSN
0040-4039
Publication Date
January 1, 1982
Volume
23
Issue
43
Start / End Page
4443 / 4446
Related Subject Headings
- Organic Chemistry
- 3405 Organic chemistry
- 3404 Medicinal and biomolecular chemistry
- 3101 Biochemistry and cell biology
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry