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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

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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.
Journal cover image

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