374073-49-1Relevant articles and documents
Synthesis of substituted indenes from isovanillin via claisen rearrangement and ring-closing metathesis
Huang, Keng-Shiang,Wang, Eng-Chi
, p. 383 - 391 (2015/02/05)
A new synthesis of substituted indenes was studied. Based on Claisen rearrangement,Wittig reaction and ring-closing metathesis (RCM), a series of substituted indenes was synthesized from isovanillin in good yields.
Synthesis of dibenzo-fused 10-membered cyclic ethers from isovanillin Via ring-closing metathesis
Wang, Eng-Chi,Lin, Yu-Li,Chen, Hsing-Ming,Li, Sie-Rong,Kabuto, Chizuko,Takeuchi, Yoshio
, p. 125 - 136 (2007/10/03)
A synthesis of substituted dibenzo-fused 10-membered cyclic ethers is described. 2-Allylbenzyl alcohols and 2-allylphenols derived from isovanillin were coupled by the Mitsunobu reaction to construct intramolecular dienes with ether linkage. The resulting
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