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D.J. Wilkins

Bio: D.J. Wilkins is an academic researcher. The author has an hindex of 1, co-authored 1 publications receiving 4 citations.

Papers
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Book ChapterDOI
TL;DR: In this paper, new developments in the field of 1,2,3-thiadiazoles have been reported along with new reactions of both the fully aromatic and reduced ring systems.
Abstract: This chapter deals with new developments in the field of 1,2,3-thiadiazoles updating the second edition covering the period 1996 to 2006. Developments in structure determination, especially X-ray structures, have been reported along with new reactions of both the fully aromatic and reduced ring systems. A new method for the preparation of 1,2,3-thiadiazoles has been included as well as recent examples of the more established methods.

4 citations


Cited by
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Journal ArticleDOI
TL;DR: The compounds 3f, 3g, 4f &4g were found to be significantly active against the tested microorganisms and the intermediates 3a-3g and bishetrocyclics 4a-4g also screened for their in vitro antimicrobial activities.

11 citations

Journal ArticleDOI
TL;DR: In this article, a cyclization of 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-yl]-5-spiro-4-acetyl-2-(acetylamino)-Δ2-1, 3, 4-thiadiazoline derivatives (3a-h) have been synthesized by the cyclization.

8 citations

Journal ArticleDOI
TL;DR: One pot synthesis of crown ether type chiral and achiral 2:2 oligomeric thiadiazolophane with (S)-BINOL and a methylene bis-naphthyl spacer unit has been achieved under simple and mild conditions by O-alkylation methodology as discussed by the authors.
Abstract: One pot synthesis of crown ether type chiral and achiral 2:2 oligomeric thiadiazolophane 1 and 3 and 3:3 oligomeric thiadiazolophane 2 and 4 with (S)-BINOL and a methylene bis-naphthyl spacer unit has been achieved under simple and mild conditions by O-alkylation methodology. Their photophysical and electrochemical properties revealed a higher degree of aggregation in 2:2 oligomer (1 and 3) and 3:3 oligomer cyclophanes 2 and 4 energy minimized calculations reveal that cyclophane with a bigger cavity has a lower heat of formation than cyclophane with a smaller cavity.

3 citations