Indenol Explained

Indenols are hydroxylated indene. 3-Indenol is an enol forms of 1-indanone, and 2-indenol is an enol form of 2-indanone. Isomerization of 1-indenol can produce 1-indanone.[1] Indenolol is a derivative of a phenolic indenol.[2]

Notes and References

  1. Connors N, Prevoznak R, Chartrain M, Reddy J, Singhvi R, Patel Z, Olewinski R, Salmon P, Wilson J, Greasham R . 6 . 10.1038/sj.jim.2900402 . Conversion of indene to cis -(1 S),(2 R)-indandiol by mutants of Pseudomonas putida F1 . 1997 . Journal of Industrial Microbiology and Biotechnology . 18 . 6 . 353–359 . 37645524 . free .
  2. Trimarco B, Cuocolo A, Groothold G, Ricciardelli B, De Luca N, Volpe M, Veniero AM, Condorelli M . 6 . Indenolol: a new antihypertensive agent: efficacy, toxicity, and hemodynamic effects in a crossover double-blind study with metoprolol . Journal of Clinical Pharmacology . 25 . 5 . 328–36 . 1985 . 4031109 . 10.1002/j.1552-4604.1985.tb02850.x . 22844379 .

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