Literature DB >> 15049634

Use of thiazoles in the halogen dance reaction: application to the total synthesis of WS75624 B.

Eric L Stangeland1, Tarek Sammakia.   

Abstract

The total synthesis of the pyridine-thiazole-containing natural product WS75624 B (1) is described. This synthesis proceeds via the Stille coupling of appropriately functionalized pyridine and thiazole components, and this paper details our studies on the use of the halogen dance reaction to prepare the desired thiazole. Various halogen dance reactions on thizoles are described, including a novel one-pot multistep reaction in which 2-bromothiazole is treated with LDA in the presence of a silyl chloride at -78 degrees C and quenched with an electrophile to provide the highly functionalized thiazole derivatives 27.

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Year:  2004        PMID: 15049634     DOI: 10.1021/jo0351217

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


  4 in total

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3.  Optimization of the central heterocycle of alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase.

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4.  Room-Temperature Asymmetric Transfer Hydrogenation of Biomass-Derived Levulinic Acid to Optically Pure γ-Valerolactone Using a Ruthenium Catalyst.

Authors:  Vaishali S Shende; Amol B Raut; Prathamesh Raghav; Ashutosh A Kelkar; Bhalchandra M Bhanage
Journal:  ACS Omega       Date:  2019-11-05
  4 in total

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