
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/1923
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jadhav, A.S. | - |
dc.contributor.author | Anand, R.V. | - |
dc.date.accessioned | 2020-11-20T04:44:45Z | - |
dc.date.available | 2020-11-20T04:44:45Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | European Journal of Inorganic Chemistry, 2017(25) | en_US |
dc.identifier.other | 10.1002/ejoc.201700587 | - |
dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201700587 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/1923 | - |
dc.description.abstract | A 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.language.iso | en_US | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Triflic Acid Catalyzed | en_US |
dc.subject | p‐Quinone | en_US |
dc.subject | Continuous‐Flow Conditions | en_US |
dc.title | Triflic Acid Catalyzed 1,6-Conjugate Addition of Thiols to p-Quinone Methides under Continuous-Flow Conditions | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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