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- W2024758167 abstract "ABC analogues of the antitumor antibiotic lavendamycin, which contain the key metal chelation site and redox-active quinone unit essential for biological activity, were prepared via the palladium(0)-catalyzed cross-coupling reaction of various 2-haloheteroaromatics with 2-stannylated pyridines and quinolines. Using the Stille reaction, 2-bromo substituted quinolines and 1-bromoisoquinolines were found to undergo efficient coupling with 2-pyridinylstannanes to provide unsymmetrical heterobiaryl derivatives. While the Stille reaction using the reverse coupling partners (i.e., 2-quinolinylstannanes and haloheteroaromatics) had not received much attention in the literature, we found that this alternative coupling reaction efficiently provided several new heterobiaryl derivatives. The gold-catalyzed intramolecular cycloisomerization of N-(prop-2-ynyl)-1H-indole-2-carboxamide smoothly afforded a β-carbolinone derivative that was subsequently used for a Pd(0)-catalyzed cross-coupling directed toward the synthesis of lavendamycin analogues." @default.
- W2024758167 created "2016-06-24" @default.
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- W2024758167 creator A5037254778 @default.
- W2024758167 creator A5060889216 @default.
- W2024758167 creator A5067641019 @default.
- W2024758167 date "2009-12-17" @default.
- W2024758167 modified "2023-10-12" @default.
- W2024758167 title "Heteroaryl Cross-Coupling as an Entry toward the Synthesis of Lavendamycin Analogues: A Model Study" @default.
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- W2024758167 cites W1973051136 @default.
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- W2024758167 cites W2008217595 @default.
- W2024758167 cites W2014573232 @default.
- W2024758167 cites W2015875329 @default.
- W2024758167 cites W2023036799 @default.
- W2024758167 cites W2024122111 @default.
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- W2024758167 doi "https://doi.org/10.1021/jo902287t" @default.
- W2024758167 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20017470" @default.
- W2024758167 hasPublicationYear "2009" @default.
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