Indenol

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]

References

^ Connors N, Prevoznak R, Chartrain M, Reddy J, Singhvi R, Patel Z, et al. (1997). "Conversion of indene to cis -(1 S ),(2 R )-indandiol by mutants of Pseudomonas putida F1". Journal of Industrial Microbiology and Biotechnology. 18 (6): 353–359. doi:10.1038/sj.jim.2900402. S2CID 37645524.
^ Trimarco B, Cuocolo A, Groothold G, Ricciardelli B, De Luca N, Volpe M, et al. (1985). "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. doi:10.1002/j.1552-4604.1985.tb02850.x. PMID 4031109. S2CID 22844379.

[1] Connors N, Prevoznak R, Chartrain M, Reddy J, Singhvi R, Patel Z, et al. (1997). "Conversion of indene to cis -(1 S ),(2 R )-indandiol by mutants of Pseudomonas putida F1". Journal of Industrial Microbiology and Biotechnology. 18 (6): 353–359. doi:10.1038/sj.jim.2900402. S2CID 37645524.

[2] Trimarco B, Cuocolo A, Groothold G, Ricciardelli B, De Luca N, Volpe M, et al. (1985). "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. doi:10.1002/j.1552-4604.1985.tb02850.x. PMID 4031109. S2CID 22844379.

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