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Volumn 48, Issue 19, 2009, Pages 3458-3461

A multicomponent reaction of arynes, isocyanides, and terminal alkynes: Highly chemo- And regioselective Synthesis of polysubsti- tuted pyridines and isoquinolines

Author keywords

Arynes; Isoquinolines; Multicomponent reactions; Pyridines; Regioselectivity

Indexed keywords

ARYNES; CHEMO-AND REGIOSELECTIVITIES; ISOCYANIDES; ISOQUINOLINES; MULTICOMPONENT REACTIONS; REACTION CONDITIONS; REGIOSELECTIVE SYNTHESIS; SYNTHETIC STRATEGIES; TERMINAL ALKYNE;

EID: 70349783775     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200900212     Document Type: Article
Times cited : (198)

References (46)
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    • The resulting aryl anion is available to abstract a proton, thus leading to the formation of monosubstituted arenes. For examples, see: a
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    • By using toluene in MeCN (as the solvent), one can slow the generation of the benzyne and therefore improve the yield of product 5a. For the details, see: Z. J. Lui, R. C. Larock, J. Org. Chem. 2007, 72, 223.
    • By using toluene in MeCN (as the solvent), one can slow the generation of the benzyne and therefore improve the yield of product 5a. For the details, see: Z. J. Lui, R. C. Larock, J. Org. Chem. 2007, 72, 223.
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    • Preferential nucleophilic attack at the para position to a chlorine atom also occurred in nucleophilic reactions with p-chloroaryne:
    • Preferential nucleophilic attack at the para position to a chlorine atom also occurred in nucleophilic reactions with p-chloroaryne:


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