Literature DB >> 11672044

Monosubstituted Oxazoles. 1. Synthesis of 5-Substituted Oxazoles by Directed Alkylation.

Cynthia M. Shafer1, Tadeusz F. Molinski.   

Abstract

A general method is presented for synthesis of 2-(methylthio)-5-substituted oxazoles 2. Deprotonation of the readily available 2-(methylthio)oxazole (1) with n-BuLi occurs smoothly in the presence of TMEDA and regiospecifically at C5. The organometallic 1a added rapidly to aldehydes and other electrophiles to provide 5-substituted-2-(methylthio)oxazoles in very good to excellent yields. Reductive removal of the MeS group gave the desired 5-monosubstituted oxazoles 3 in good yield.

Entities:  

Year:  1998        PMID: 11672044     DOI: 10.1021/jo971410h

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  5 in total

1.  Efficient Suzuki and Stille Reactions for Regioselective Strategies of Incorporation of the 1,3-Oxazole Heterocycle. Mild Desulfonylation for the Synthesis of C-4 and C-5 Monosubstituted Oxazoles.

Authors:  David R Williams; Liangfeng Fu
Journal:  Synlett       Date:  2010-07-01       Impact factor: 2.454

Review 2.  The oxazolomycin family: a review of current knowledge.

Authors:  Patrik Oleksak; Jozef Gonda; Eugenie Nepovimova; Kamil Kuca; Kamil Musilek
Journal:  RSC Adv       Date:  2020-11-09       Impact factor: 4.036

3.  General methodology for the preparation of 2,5-disubstituted-1,3-oxazoles.

Authors:  David R Williams; Liangfeng Fu
Journal:  Org Lett       Date:  2010-02-19       Impact factor: 6.005

4.  Internal azomethine ylide cycloaddition methodology for access to the substitution pattern of aziridinomitosene A.

Authors:  Drew R Bobeck; Don L Warner; Edwin Vedejs
Journal:  J Org Chem       Date:  2007-10-02       Impact factor: 4.354

5.  Synthesis and structure-activity relationships of bengazole A analogs.

Authors:  Roger J Mulder; Cynthia M Shafer; Doralyn S Dalisay; Tadeusz F Molinski
Journal:  Bioorg Med Chem Lett       Date:  2009-04-22       Impact factor: 2.823

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.