79928-74-8Relevant articles and documents
Syntheses of substituted naphthalenes and naphthols
Huang, Keng-Shiang,Wang, Eng-Chi,Chen, Hsing-Ming
, p. 585 - 605 (2007/10/03)
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
Vilsmeier-Haack Reaction on Methoxyallylbenzenes
Narasimhan, N. S.,Mukhopadhyay, T.,Kusurkar, S. S.
, p. 546 - 548 (2007/10/02)
Vilsmeier-Haack reaction on various methoxyallylbenzenes yields the naphthaldehydes (2, 11, 14, 17, 20, 21) when ortho-position to the allyl group is activated.In other cases only nuclear formylated products are obtained.The product analysis suggests that nuclear formylation is probably the first step in these reactions.