
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2663
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DC Field | Value | Language |
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dc.contributor.author | Jadhav, A.S. | - |
dc.contributor.author | Anand, R.V. | - |
dc.date.accessioned | 2020-12-04T06:38:15Z | - |
dc.date.available | 2020-12-04T06:38:15Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Organic and Biomolecular Chemistry, 15(1), pp. 56-60. | en_US |
dc.identifier.other | https://doi.org/10.1039/C6OB02277D | - |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2017/ob/c6ob02277d#!divAbstract | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2663 | - |
dc.description.abstract | An efficient method for the synthesis of alkyl diarylmethanes through the 1,6-conjugate addition of dialkylzinc reagents to para-quinone methides (p-QMs) has been developed under continuous flow conditions using a microreactor. This protocol allows to access unsymmetrical alkyl diarylmethanes in moderate to excellent yields using a wide range of p-QMs and dialkylzinc reagents. Interestingly, this transformation worked well without the requirement of a catalyst. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.subject | Dialkylzinc | en_US |
dc.subject | Efficient | en_US |
dc.subject | Synthesis | en_US |
dc.title | 1,6-Conjugate addition of zinc alkyls to para-quinone methides in a continuous-flow microreactor† | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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