2017
DOI: 10.1002/jlcr.3480
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Tritium-labelled alkaloids: Synthesis and applications

Abstract: This review discusses the synthetic methods used to tritiate nonmorphinan alkaloids as well as their applications.

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Cited by 10 publications
(3 citation statements)
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References 174 publications
(285 reference statements)
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“…Five years ago, Filer published a review [88] dedicated to the synthesis and applications of the tritium-labeled [75] with the permission of Springer Nature alkaloids including indole alkaloids Reproduced with minor editing privilege from Vogt et al [83] with the permission of John Wiley and Sons enumeration of alkaloids is taken from the parent review). The author stated that "the extreme structural and functional variety of alkaloids has presented both valuable opportunities and complex synthetic challenges for their tritiation.…”
Section: Recent and Most Recent Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Five years ago, Filer published a review [88] dedicated to the synthesis and applications of the tritium-labeled [75] with the permission of Springer Nature alkaloids including indole alkaloids Reproduced with minor editing privilege from Vogt et al [83] with the permission of John Wiley and Sons enumeration of alkaloids is taken from the parent review). The author stated that "the extreme structural and functional variety of alkaloids has presented both valuable opportunities and complex synthetic challenges for their tritiation.…”
Section: Recent and Most Recent Resultsmentioning
confidence: 99%
“…Five years ago, Filer published a review [ 88 ] dedicated to the synthesis and applications of the tritium‐labeled alkaloids including indole alkaloids 1 – 6 , 8 ; quinoline and isoquinoline alkaloids 11 – 16 ; pyridine alkaloids 17 – 19 ; isoxazole alkalpids 20 – 22 ; tropane alkaloids exemplified with 23 ; pyrrolizidine alkaloids exemplified with 24 ; quinolizidine alkaloids 25 , 27 ; piperidine alkaloids exemplified with 28 ; steroidal alkaloids exemplified with 29 ; amaryllidaceae alkaloids 30 , 31 ; tropolone protoalkaloid 32 ; and marine toxin alkaloids 33 – 35 (for clarity, enumeration of alkaloids is taken from the parent review). The author stated that “the extreme structural and functional variety of alkaloids has presented both valuable opportunities and complex synthetic challenges for their tritiation.…”
Section: Recent and Most Recent Resultsmentioning
confidence: 99%
“…Pure isocyanic acid was retained in the middle trap, and its quality was checked with gas‐phase IR spectroscopy (Bruker, Tensor 27). Isotopically‐labelled HN 13 CO and H 15 NCO were prepared from 13 C and 15 N‐labelled potassium cyanate, which were synthesized via reactions of potassium phenoxide with 13 C and 15 N‐labelled urea according to the literature procedure [21] …”
Section: Methodsmentioning
confidence: 99%