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Published in 2024 at "Organic letters"
DOI: 10.1021/acs.orglett.4c03016
Abstract: 4-Quinolone derivatives undergo an unexpected ring expansion reaction with α-halo esters/phosphonates/sulfones in the presence of a base, such as NaH, to produce novel benzazepinones. Under these mild and transition-metal-free conditions, most substrates gave moderate to…
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Keywords:
reaction;
expansion reaction;
base promoted;
promoted ring ... See more keywords
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Published in 2019 at "Chemical communications"
DOI: 10.1039/c9cc03375k
Abstract: The FeCl3-promoted ring size-controlled oxidative activation of o-alkynylanilines opens up a complementary appealing protocol for poly-N-heterocycle synthesis. When electron-poor π-alkyne iron species combine with cyclic enamines obtained from cyclohexanone and β-tetralone, they undergo a regioselective…
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Keywords:
size dictating;
ring size;
promoted ring;
fecl3 promoted ... See more keywords
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Published in 2021 at "Organic Chemistry Frontiers"
DOI: 10.1039/d1qo00770j
Abstract: In an unusual cascade process involving KCN, vinyl cyclic carbonates are converted into β-cyano ketones with the subsequent extrusion of carbon dioxide and acetonitrile facilitating a Michael addition to an intermediate α,β-unsaturated ketone.
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Keywords:
cyano ketones;
ketones cyanide;
formation cyano;
promoted ring ... See more keywords
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Published in 2024 at "Organic Chemistry Frontiers"
DOI: 10.1039/d4qo01632g
Abstract: An efficient protocol for the synthesis of [4.6] spirocarbocycles has been developed. This process is realized through the sequential K2CO3-promoted C−C σ-bond cleavage of cyclic ketoesters and an I2-mediated selective...
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Keywords:
synthesis spirocarbocycles;
spirocarbocycles base;
protocol;
promoted ring ... See more keywords