Literature DB >> 12783504

Lewis acid catalyzed room-temperature Michaelis-Arbuzov rearrangement.

Pierre-Yves Renard1, Philippe Vayron, Eric Leclerc, Alain Valleix, Charles Mioskowski.   

Abstract

Entities:  

Year:  2003        PMID： 12783504     DOI： 10.1002/anie.200250270

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  6 in total

1.  Synthesis of α-Arylphosphonates Using Copper-Catalyzed α-Arylation and Deacylative α-Arylation of β-Ketophosphonates.

Authors:  Laxmidhar Rout; Sridhar Regati; Cong-Gui Zhao
Journal:  Adv Synth Catal       Date:  2011-12-06       Impact factor: 5.837

2.  Room-temperature alternative to the Arbuzov reaction: the reductive deoxygenation of acyl phosphonates.

Authors:  Sean M A Kedrowski; Dennis A Dougherty
Journal:  Org Lett       Date:  2010-09-17       Impact factor: 6.005

3.  Linking Molecular Structure via Functional Group to Chemical Literature for Establishing a Reaction Lineage for Application to Alternatives Assessment.

Authors:  William M Barrett; Sudhakar Takkellapati; Kidus Tadele; Todd M Martin; Michael A Gonzalez
Journal:  ACS Sustain Chem Eng       Date:  2019-04-15       Impact factor: 8.198

4.  Direct conversion of benzylic and allylic alcohols to phosphonates.

Authors:  Rocky J Barney; Rebekah M Richardson; David F Wiemer
Journal:  J Org Chem       Date:  2011-03-15       Impact factor: 4.354

5.  Direct phosphorylation of benzylic C-H bonds under transition metal-free conditions forming sp3C-P bonds.

Authors:  Qiang Li; Chang-Qiu Zhao; Tieqiao Chen; Li-Biao Han
Journal:  RSC Adv       Date:  2022-06-24       Impact factor: 4.036

Review 6.  Improvements, Variations and Biomedical Applications of the Michaelis-Arbuzov Reaction.

Authors:  Stavroula Kostoudi; Georgios Pampalakis
Journal:  Int J Mol Sci       Date:  2022-03-21       Impact factor: 5.923
  6 in total

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