Literature DB >> 17637848

An Economic and Practical Synthesis of the 2-Tetrahydrofuranyl Ether Protective Group.

J R Falck, De Run Li, Romain Bejot, Charles Mioskowski.   

Abstract

Primary, secondary, and tertiary alcohols as well as phenols and carbohydrates are efficiently transformed into the corresponding 2-tetrahydrofuranyl ethers by a combination of Mn(0) powder and CCl(4) in tetrahydrofuran.

Entities:  

Year:  2006        PMID： 17637848      PMCID： PMC1827073          DOI： 10.1016/j.tetlet.2006.05.081

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN： 0040-4039            Impact factor:   2.415


  2 in total

1.  Tuning reactivity and chemoselectivity in electron transfer initiated cyclization reactions: applications to carbon-carbon bond formation.

Authors:  John R Seiders; Lijun Wang; Paul E Floreancig
Journal:  J Am Chem Soc       Date:  2003-03-05       Impact factor: 15.419

2.  A convenient synthesis of 2-tetrahydrofuranyl ethers.

Authors:  R Baati; A Valleix; C Mioskowski; D K Barma; J R Falck
Journal:  Org Lett       Date:  2000-02-24       Impact factor: 6.005
  2 in total
  1 in total

Review 1.  Naturally Occurring and Artificial N9-Cytokinin Conjugates: From Synthesis to Biological Activity and Back.

Authors:  Hana Vylíčilová; Magdaléna Bryksová; Vlasta Matušková; Karel Doležal; Lucie Plíhalová; Miroslav Strnad
Journal:  Biomolecules       Date:  2020-05-29
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.