Syntheses of substituted naphthalenes and naphthols

KS Huang, EC Wang, HM Chen

Index: Huang, Keng-Shiang; Wang, Eng-Chi; Chen, Hsing-Ming Journal of the Chinese Chemical Society, 2004 , vol. 51, # 3 p. 585 - 605

Full Text: HTML

Citation Number: 13

Abstract

Abstract Syntheses of substituted naphthalenes and naphthols are described. Based on Claisen rearrangement, ring-closing metathesis (RCM), and related reactions, isovanillin was successfully transformed into a series of substituted naphthalenes and naphthols with good overall yields.

Related Articles:

Product and mechanistic studies of the anodic oxidation of methoxylated naphthalenes. The EECrCp mechanism

[Dolson,M.G.; Swenton,J.S. Journal of the American Chemical Society, 1981 , vol. 103, p. 2361]

Product and mechanistic studies of the anodic oxidation of methoxylated naphthalenes. The EECrCp mechanism

[Dolson,M.G.; Swenton,J.S. Journal of the American Chemical Society, 1981 , vol. 103, p. 2361]

Product and mechanistic studies of the anodic oxidation of methoxylated naphthalenes. The EECrCp mechanism

[Dolson,M.G.; Swenton,J.S. Journal of the American Chemical Society, 1981 , vol. 103, p. 2361]

Eine neuc Umlagerung an einem Metathebainon-Derivat mit Cyclohexa-2, 5-dienon-Struktur

[Fleischhacker,W.; Vieboeck,F. Monatshefte fuer Chemie, 1969 , vol. 100, # 1 p. 163 - 174]

More Articles...