Perhydroindanone derivatives. II. Stability relationships
HO House, GH Rasmusson
Index: House,H.O.; Rasmusson,G.H. Journal of Organic Chemistry, 1963 , vol. 28, p. 31 - 34
Full Text: HTML
Citation Number: 38
Abstract
(4) Although the product characterization was rather fragmentary, this reaction has been reported by E. Dane and K. Eder, Ann., 639, 207 (1939).(2) with cyclopeiitenone (I), partial equilibration of the expected, kinetically favored isomer 45 with its epimer 5 was observed, the equilibration being more nearly complete at higher temperatures. The corresponding reaction with piperylene could be effected at lower temperature; the expected5 cis isomer ...
Related Articles:
[Levy, Jean-Noel; Latham, Christopher M.; Roisin, Loic; Kandziora, Nadine; Fruscia, Paolo Di; White, Andrew J. P.; Woodward, Simon; Fuchter, Matthew J. Organic and Biomolecular Chemistry, 2012 , vol. 10, # 3 p. 512 - 515]
[Bednarek; Zhu; Bally; Filipiak; Marcinek; Gebicki Journal of the American Chemical Society, 2001 , vol. 123, # 10 p. 2377 - 2387]
[Kobayashi, Toyoharu; Tanaka, Katsunori; Miwa, Junichi; Katsumura, Shigeo Tetrahedron Asymmetry, 2004 , vol. 15, # 2 p. 185 - 188]
An NMR investigation of the Mills-Nixon effect
[Collins, Michael J.; Gready, Jill E.; Sternhell, Sever; Tansey, Charles W. Australian Journal of Chemistry, 1990 , vol. 43, p. 1547 - 1557]
Synthesis of indanones via solid-supported [2+ 2+ 2] cyclotrimerization
[Senaiar, Ramesh S.; Teske, Jesse A.; Young, Douglas D.; Deiters, Alexander Journal of Organic Chemistry, 2007 , vol. 72, # 20 p. 7801 - 7804]