Literature DB >> 21796696

Rapid access to α-alkoxy and α-amino acid derivatives through safe continuous-flow generation of diazoesters.

Hannah E Bartrum1, David C Blakemore, Christopher J Moody, Christopher J Hayes.   

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Year:  2011        PMID： 21796696     DOI： 10.1002/chem.201101590

Source DB:  PubMed          Journal:  Chemistry        ISSN： 0947-6539            Impact factor:   5.236


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  5 in total

1.  Highly stereoselective C-C bond formation by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and chiral allylic alcohols.

Authors:  Zhanjie Li; Brendan T Parr; Huw M L Davies
Journal:  J Am Chem Soc       Date:  2012-06-25       Impact factor: 15.419

2.  The combined C-H functionalization/Cope rearrangement: discovery and applications in organic synthesis.

Authors:  Huw M L Davies; Yajing Lian
Journal:  Acc Chem Res       Date:  2012-05-11       Impact factor: 22.384

3.  Potassium N-iodo p-toluenesulfonamide (TsNIK, Iodamine-T): a new reagent for the oxidation of hydrazones to diazo compounds.

Authors:  Simon M Nicolle; Christopher J Moody
Journal:  Chemistry       Date:  2014-03-11       Impact factor: 5.236

4.  Ethyl diazoacetate synthesis in flow.

Authors:  Mariëlle M E Delville; Jan C M van Hest; Floris P J T Rutjes
Journal:  Beilstein J Org Chem       Date:  2013-09-05       Impact factor: 2.883

Review 5.  Generation of Tosyl Azide in Continuous Flow Using an Azide Resin, and Telescoping with Diazo Transfer and Rhodium Acetate-Catalyzed O-H Insertion.

Authors:  Rosella M O'Mahony; Denis Lynch; Katie S O'Callaghan; Stuart G Collins; Anita R Maguire
Journal:  Org Process Res Dev       Date:  2021-11-30       Impact factor: 3.317
  5 in total

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