Triflic Acid Catalyzed 1,6-Conjugate Addition of Thiols to p-Quinone Methides under Continuous-Flow Conditions

dc.contributor.authorJadhav, A.S.
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-11-20T04:44:45Z
dc.date.available2020-11-20T04:44:45Z
dc.date.issued2017
dc.description.abstractA 100 % atom‐efficient continuous‐flow protocol to access diarylmethyl thioethers through the triflic acid (TfOH) catalyzed 1,6‐conjugate addition of thiols to p‐quinone methides by using microreactor technology is developed. image Abstract A simple and efficient protocol to access diarylmethyl thioethers through the triflic acid catalyzed vinylogous Michael addition of aromatic and aliphatic thiols to p‐quinone methides under continuous‐flow conditions by using a microreactor was developed.en_US
dc.identifier.citationEuropean Journal of Inorganic Chemistry, 2017(25)en_US
dc.identifier.other10.1002/ejoc.201700587
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201700587
dc.identifier.urihttp://hdl.handle.net/123456789/1923
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.subjectTriflic Acid Catalyzeden_US
dc.subjectp‐Quinoneen_US
dc.subjectContinuous‐Flow Conditionsen_US
dc.titleTriflic Acid Catalyzed 1,6-Conjugate Addition of Thiols to p-Quinone Methides under Continuous-Flow Conditionsen_US
dc.typeArticleen_US

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