Literature DB >> 10891172

Protecting Groups for Thiols Suitable for Suzuki Conditions.

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Abstract

The thiol group is one of the few groups NOT tolerated by the Suzuki reaction. Therefore, a new protective group, the 2-methoxyisobutyryl group, was developed by tuning the electronic/steric properties of the acyl residue. Other thioesters, such as thioacetate, result in a more or less dominant side reaction, which to date has not been described: sulfur-assisted acylation of boronic acids. The reaction pathway for this new reaction is discussed.

Entities:  

Year:  2000        PMID: 10891172     DOI: 10.1021/ol0058902

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  A Modular Synthesis of Teraryl-Based α-Helix Mimetics, Part 5: A Complete Set of Pyridine Boronic Acid Pinacol Esters Featuring Side Chains of Proteinogenic Amino Acids.

Authors:  Melanie Trobe; Till Schreiner; Martin Vareka; Sebastian Grimm; Bernhard Wölfl; Rolf Breinbauer
Journal:  European J Org Chem       Date:  2022-02-24

2.  A Modular Synthesis of Teraryl-Based α-Helix Mimetics, Part 4: Core Fragments with Two Halide Leaving Groups Featuring Side Chains of Proteinogenic Amino Acids.

Authors:  Melanie Trobe; Julia Blesl; Martin Vareka; Till Schreiner; Rolf Breinbauer
Journal:  European J Org Chem       Date:  2022-02-24

3.  Controlled Selectivity through Reversible Inhibition of the Catalyst: Stereodivergent Semihydrogenation of Alkynes.

Authors:  Jie Luo; Yaoyu Liang; Michael Montag; Yael Diskin-Posner; Liat Avram; David Milstein
Journal:  J Am Chem Soc       Date:  2022-07-15       Impact factor: 16.383

  3 in total

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