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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b03059
Abstract: A general approach to access sulfamate esters through preparation of sulfamic acid salts, subsequent activation with triphenylphosphine ditriflate, and nucleophilic trapping is disclosed. The method proceeds in modest to excellent yields to incorporate nucleophiles derived…
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Keywords:
acid salts;
sulfamate esters;
activation triphenylphosphine;
triphenylphosphine ditriflate ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b02621
Abstract: A general method is described for the coupling of (hetero)aryl bromides with O-alkyl sulfamate esters. The protocol relies on catalytic amounts of nickel and photoexcitable iridium complexes and proceeds under visible light irradiation at ambient…
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Keywords:
hetero aryl;
alkyl sulfamate;
sulfamate;
sulfamate esters ... See more keywords
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Published in 2023 at "Chemical Science"
DOI: 10.1039/d2sc05945b
Abstract: Sulfur(vi) fluoride exchange chemistry has been reported to be effective at synthesizing valuable sulfur(vi) functionalities through sequential nucleophilic additions, yet oxygen-based nucleophiles are limited in this approach to phenolic derivatives. Herein, we report a new…
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Keywords:
sulfur fluoride;
sulfamate esters;
chemistry;
sulfur ... See more keywords