Unknown

Dataset Information

0

UV-Induced 1,3,4-Oxadiazole Formation from 5-Substituted Tetrazoles and Carboxylic Acids in Flow.


ABSTRACT: A range of 1,3,4-oxadiazoles have been synthesized using a UV-B activated flow approach starting from carboxylic acids and 5-substituted tetrazoles. The application of UV light represents an attractive alternative to the traditional thermolytic approach and has demonstrated comparable efficiency and versatility, with a diverse substrate scope, including the incorporation of highly substituted amino acids.

SUBMITTER: Green L 

PROVIDER: S-EPMC7756889 | biostudies-literature | 2020 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

UV-Induced 1,3,4-Oxadiazole Formation from 5-Substituted Tetrazoles and Carboxylic Acids in Flow.

Green Luke L   Livingstone Keith K   Bertrand Sophie S   Peace Simon S   Jamieson Craig C  

Chemistry (Weinheim an der Bergstrasse, Germany) 20201012 65


A range of 1,3,4-oxadiazoles have been synthesized using a UV-B activated flow approach starting from carboxylic acids and 5-substituted tetrazoles. The application of UV light represents an attractive alternative to the traditional thermolytic approach and has demonstrated comparable efficiency and versatility, with a diverse substrate scope, including the incorporation of highly substituted amino acids. ...[more]

Similar Datasets

| S-EPMC10779255 | biostudies-literature
| S-EPMC9313617 | biostudies-literature
| S-EPMC4142979 | biostudies-literature
| S-EPMC3152068 | biostudies-literature
| S-EPMC3463135 | biostudies-literature
| S-EPMC4661007 | biostudies-literature
| S-EPMC3011497 | biostudies-literature
| S-EPMC3120570 | biostudies-literature
| S-EPMC3239005 | biostudies-literature
| S-EPMC8148175 | biostudies-literature