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Published in 2019 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2019.02.041
Abstract: Graphical abstract Herein, we report an efficient new method for iodination of terminal alkynes using stoichiometric KI and CuSO4 in acetate buffer that holds promise for further development into a method for radio-iodination.
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Keywords:
iodination;
iodination terminal;
terminal alkynes;
method ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02695
Abstract: A photoredox thioformylation of terminal alkynes using nitromethane as a formyl anion equivalent, thereby leading to the synthesis of (E)-1,2-difunctionalized acrylaldehyde, has been described. The current strategy introduces an adaptable aldehyde function across an alkyne…
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Keywords:
thioformylation terminal;
nitromethane formyl;
using nitromethane;
terminal alkynes ... See more keywords
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Published in 2020 at "Organic chemistry frontiers"
DOI: 10.1039/d0qo00367k
Abstract: We have developed a highly regioselective halothiolation of alkynes under simple and mild conditions. Our halothiolation reagents are readily available alkali metal halides and N-thiosuccinimides. Our transition metal-free system offers good chemical yields for a…
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Keywords:
halides thiosuccinimides;
halothiolation;
regio stereoselective;
stereoselective halothiolation ... See more keywords
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Published in 2023 at "Molecules"
DOI: 10.3390/molecules28083433
Abstract: Dehydrogenative borylation of terminal alkynes has recently emerged as an atom-economical one-step alternative to traditional alkyne borylation methodologies. Using lithium aminoborohydrides, formed in situ from the corresponding amine-boranes and n-butyllithium, a variety of aromatic and…
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Keywords:
alkynes using;
lithium aminoborohydrides;
lithium;
terminal alkynes ... See more keywords