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Published in 2019 at "ChemCatChem"
DOI: 10.1002/cctc.201901933
Abstract: We have developed a highly effective palladium/PHOX catalyst system for efficient asymmetric 1,2‐addition of arylboronic acids to six‐membered 1,2,6‐thiadiazine‐1,1‐dioxide type cyclic N‐sulfonyl α‐iminoesters. The protocol allows convenient synthesis of a variety of nearly optically pure…
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Keywords:
synthesis;
amino acid;
acid derivatives;
cyclic sulfonyl ... See more keywords
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Published in 2017 at "European Journal of Organic Chemistry"
DOI: 10.1002/ejoc.201700569
Abstract: A new strategy has been developed for the first time for the synthesis of spirofluorenyl benzosultams through the annulation of aryl iodides with cyclic N-sulfonyl ketimines. This method involves a readily available Pd(II) catalyst for…
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Keywords:
pdii catalyzed;
aryl iodides;
catalyzed spiroannulation;
activation ... See more keywords
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Published in 2020 at "Science China Chemistry"
DOI: 10.1007/s11426-019-9760-7
Abstract: A diastereoselectivity-controllable formal [3+2]-cycloaddition of arylvinyl oxirane 2,2-diesters with cyclic N-sulfonyl imines is developed, affording the corresponding tricyclic oxazolidine derivatives in moderate to excellent yields with excellent diastereoselectivities in the presence of palladium(0) or scandium(III)…
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Keywords:
catalyst controlled;
sulfonyl imines;
oxirane diesters;
cyclic sulfonyl ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b01732
Abstract: Cyclic sulfonamides (sultams) play a unique role in drug discovery and synthetic chemistry. A direct synthesis of sultams by an intramolecular C(sp3)-H amidation reaction using an iron complex in situ derived from Fe(ClO4)2 and aminopyridine…
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Keywords:
iron catalyzed;
synthesis sultams;
cyclic sulfonyl;
iron ... See more keywords