2016
DOI: 10.1016/j.tetlet.2016.10.075
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One-pot reaction of pyranoindolones with phenylisocyanates: a simple and regioselective approach to β-carbolines

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Cited by 2 publications
(1 citation statement)
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“…The ability of the borane-water adduct to donate a proton is as strong as HCl (pK a = 8.4/8.5 in MeCN). [7] Isocyanates are known to be reactive electrophiles [8] which undergo a range of reactions with various nucleophiles, such as amines to produce carbodiimides, [9][10][11] as exemplified by the hydroamination of isocyanates which produces functionalised urea derivatives. [12][13][14] This class of scaffolds has been identified as important building blocks towards pharmaceuticals, [15] agrochemicals, [16] and in materials chemistry.…”
mentioning
confidence: 99%
“…The ability of the borane-water adduct to donate a proton is as strong as HCl (pK a = 8.4/8.5 in MeCN). [7] Isocyanates are known to be reactive electrophiles [8] which undergo a range of reactions with various nucleophiles, such as amines to produce carbodiimides, [9][10][11] as exemplified by the hydroamination of isocyanates which produces functionalised urea derivatives. [12][13][14] This class of scaffolds has been identified as important building blocks towards pharmaceuticals, [15] agrochemicals, [16] and in materials chemistry.…”
mentioning
confidence: 99%