2, 5-Di-t-butyl-4-methoxyphenol and 2, 6-Di-t-butyl-4-methoxyphenol
CD Cook, RG Inskeep, AS Rosenberg…
Index: Cook et al. Journal of the American Chemical Society, 1955 , vol. 77, p. 1672
Full Text: HTML
Citation Number: 9
Abstract
ation with tetranitromethane and lack of high-intensity absorption in the ultraviolet. Only one structure (I) seems to accommodate these facts and to be consistent with the conditions of the transformation. The attachment of the cholestene moiety to Cz follows from the preferred direction
Related Articles:
[Kulkarni, Mukund G.; Kate, Sandesh D. Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 24 p. 4242 - 4244]
[Ng, Eng-Poh; Mohd Subari, Siti Norbayu; Marie, Olivier; Mukti, Rino R.; Juan, Joon-Ching Applied Catalysis A: General, 2013 , vol. 450, p. 34 - 41]
[Ng, Eng-Poh; Mohd Subari, Siti Norbayu; Marie, Olivier; Mukti, Rino R.; Juan, Joon-Ching Applied Catalysis A: General, 2013 , vol. 450, p. 34 - 41]
[Selassie, Cynthia D.; Verma, Rajeshwar P.; Kapur, Sanjay; Shusterman, Alan J.; Hansch, Corwin Journal of the Chemical Society. Perkin Transactions 2, 2002 , # 6 p. 1112 - 1117]
Oxidation of catechol and of 2, 6-di-tert-butylphenol by dioxiranes
[Altamura; Fusco; D'Accolti; Mello; Prencipe; Curci Tetrahedron Letters, 1991 , vol. 32, # 40 p. 5445 - 5448]