812646-68-7Relevant academic research and scientific papers
Synthesis of substituted indenes from isovanillin via claisen rearrangement and ring-closing metathesis
Huang, Keng-Shiang,Wang, Eng-Chi
, p. 383 - 391 (2007/10/03)
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.
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
A synthesis of substituted 3,6-dihydro-1H-benzo[c]oxocines via Claisen rearrangement and ring-closing metathesis
Wang, Eng-Chi,Wang, Chin-Cheng,Hsu, Ming-Kun,Huang, Keng-Shiang
, p. 2021 - 2033 (2007/10/03)
Started from isovanillin, based on Claisen rearrangement and ring-closing metathesis (RCM) reaction, a series of substituted 3,6-dihydro-1H-benzo[c]oxocines were synthesized in moderate yields.
A novel synthesis of substituted naphthalenes via Claisen rearrangement and RCM reaction
Huang, Keng-Shiang,Wang, Eng-Chi
, p. 6155 - 6157 (2007/10/03)
A novel synthesis of substituted naphthalenes was studied. Starting from isovanillin, basing on Claisen rearrangement and ring-closing metathesis (RCM), a series of 1-alkoxy-2-methoxynaphthalenes and 1-alkoxy-2-methoxy-8-methylnaphthalenes together with a
