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- W2171949320 endingPage "2859" @default.
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- W2171949320 abstract "Abstract An asymmetric organocatalyzed reaction sequence involving a Michael addition of various 1,3‐dicarbonyl compounds to α,β‐unsaturated aldehydes with subsequent diastereoselective Pictet–Spengler cyclization has been developed. The substrate scope was found to be general and optically active indoloquinolizidines were isolated as single diastereomers in high yields with high to excellent enantioselectivites. In addition to tryptamine, the reaction has also been successfully applied to other nucleophiles including o ‐aminobenzylamine and anthranilamide giving rise to pyridoquinauolines and quinazolinones." @default.
- W2171949320 created "2016-06-24" @default.
- W2171949320 creator A5023705098 @default.
- W2171949320 creator A5071153001 @default.
- W2171949320 creator A5080612612 @default.
- W2171949320 creator A5090596645 @default.
- W2171949320 date "2011-10-01" @default.
- W2171949320 modified "2023-10-13" @default.
- W2171949320 title "General and Efficient Organocatalytic Synthesis of Indoloquinolizidines, Pyridoquinazolines and Quinazolinones through a One‐Pot Domino Michael Addition‐Cyclization‐ Pictet–Spengler or 1,2‐Amine Addition Reaction" @default.
- W2171949320 cites W1516205559 @default.
- W2171949320 cites W1965395588 @default.
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- W2171949320 cites W1992930332 @default.
- W2171949320 cites W1993078319 @default.
- W2171949320 cites W1996608836 @default.
- W2171949320 cites W1998372912 @default.
- W2171949320 cites W1999565233 @default.
- W2171949320 cites W2004081456 @default.
- W2171949320 cites W2008138925 @default.
- W2171949320 cites W2009617887 @default.
- W2171949320 cites W2017282825 @default.
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- W2171949320 doi "https://doi.org/10.1002/adsc.201100258" @default.
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