Five vs six membered ring formation in the vinyl radical cyclization
Publication
, Journal Article
Stork, G; Mook, R
Published in: Tetrahedron Letters
January 1, 1986
The ratio of methylenecyclopentane to methylenecyclohexane derivatives observed in the vinyl radical cyclization increases with the concentration of substrate and tin hydride. This is interpreted to mean that these cyclizations are under thermodynamic control at low concentrations. © 1986.
Duke Scholars
Published In
Tetrahedron Letters
DOI
ISSN
0040-4039
Publication Date
January 1, 1986
Volume
27
Issue
38
Start / End Page
4529 / 4532
Related Subject Headings
- Organic Chemistry
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry
Citation
APA
Chicago
ICMJE
MLA
NLM
Stork, G., & Mook, R. (1986). Five vs six membered ring formation in the vinyl radical cyclization. Tetrahedron Letters, 27(38), 4529–4532. https://doi.org/10.1016/S0040-4039(00)84995-3
Stork, G., and R. Mook. “Five vs six membered ring formation in the vinyl radical cyclization.” Tetrahedron Letters 27, no. 38 (January 1, 1986): 4529–32. https://doi.org/10.1016/S0040-4039(00)84995-3.
Stork G, Mook R. Five vs six membered ring formation in the vinyl radical cyclization. Tetrahedron Letters. 1986 Jan 1;27(38):4529–32.
Stork, G., and R. Mook. “Five vs six membered ring formation in the vinyl radical cyclization.” Tetrahedron Letters, vol. 27, no. 38, Jan. 1986, pp. 4529–32. Scopus, doi:10.1016/S0040-4039(00)84995-3.
Stork G, Mook R. Five vs six membered ring formation in the vinyl radical cyclization. Tetrahedron Letters. 1986 Jan 1;27(38):4529–4532.
Published In
Tetrahedron Letters
DOI
ISSN
0040-4039
Publication Date
January 1, 1986
Volume
27
Issue
38
Start / End Page
4529 / 4532
Related Subject Headings
- Organic Chemistry
- 0305 Organic Chemistry
- 0304 Medicinal and Biomolecular Chemistry