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Published in 2018 at "Chemical communications"
DOI: 10.1039/c8cc03612h
Abstract: The synthesis of various substituted 1H-indazoles is reported through N-N bond formation from an iminophosphorane derivative. Supported by control experiments, an original Staudinger-aza-Wittig tandem mechanism is proposed for this transformation.
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Keywords:
staudinger aza;
aza wittig;
bond formation;
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Published in 2019 at "Synlett"
DOI: 10.1055/s-0037-1610688
Abstract: A facile synthetic approach to access of 3H-pyrrolo[2,3-c]quinoline derivatives has been achieved by a sequential I2-promoted cyclization/Staudinger/aza-Wittig/dehydroaromatization reaction. The targeted products were received in moderate to good yields (62–81%). The broad substrate scope and easy…
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Keywords:
pyrrolo quinoline;
sequential promoted;
staudinger aza;
cyclization staudinger ... See more keywords
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Published in 2022 at "Molecules"
DOI: 10.3390/molecules27238130
Abstract: Realization of the one-pot Staudinger/aza-Wittig/Castagnoli–Cushman reaction sequence for a series of azido aldehydes and homophthalic anhydrides is described. The reaction proceeded at room temperature and delivered novel polyheterocycles related to the natural product realm in…
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Keywords:
staudinger aza;
wittig castagnoli;
aza wittig;
one pot ... See more keywords
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Published in 2022 at "Beilstein Journal of Organic Chemistry"
DOI: 10.3762/bjoc.18.32
Abstract: A new efficient synthesis of polysubstituted 3,4-dihydroquinazolines and 4H-3,1-benzothiazines via sequential Passerini/Staudinger/aza-Wittig/addition/nucleophilic substitution reaction has been developed. The three-component Passerini reactions of 2-azidobenzaldehydes 1, benzoic acid (2), and isocyanides 3 produced the azide intermediates 4,…
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Keywords:
aza wittig;
dihydroquinazolines benzothiazines;
passerini staudinger;
staudinger aza ... See more keywords