Matches in SemOpenAlex for { <https://semopenalex.org/work/W3033767026> ?p ?o ?g. }
- W3033767026 endingPage "4887" @default.
- W3033767026 startingPage "4883" @default.
- W3033767026 abstract "A three-component annulation reaction of N-alkyl anilines, cyclic 1,3-dicarbonyl compounds, and aryl aldehydes to julolidines and lilolidines is reported. The 6π-electrocyclization enabled the annulation to proceed with reversed regioselectivity as compared with the annulation that occurs in the Povarov reaction. Both cyclic and acyclic N-alkyl anilines participated in the reaction to provide a wide range of julolidines and lilolidines as the single regio- and diastereoisomers in good to excellent yields." @default.
- W3033767026 created "2020-06-12" @default.
- W3033767026 creator A5002154913 @default.
- W3033767026 creator A5042809027 @default.
- W3033767026 creator A5035845096 @default.
- W3033767026 date "2020-06-10" @default.
- W3033767026 modified "2023-10-14" @default.
- W3033767026 title "Diastereoselective and Reversed Regioselective Annulations of <i>N</i>-Alkyl Anilines to Julolidines and Lilolidines" @default.
- W3033767026 cites W1906854950 @default.
- W3033767026 cites W1963902907 @default.
- W3033767026 cites W1964438155 @default.
- W3033767026 cites W1965625490 @default.
- W3033767026 cites W1965858053 @default.
- W3033767026 cites W1966389206 @default.
- W3033767026 cites W1966922056 @default.
- W3033767026 cites W1970754698 @default.
- W3033767026 cites W1973923747 @default.
- W3033767026 cites W1975443028 @default.
- W3033767026 cites W1976232356 @default.
- W3033767026 cites W1981727250 @default.
- W3033767026 cites W1992304492 @default.
- W3033767026 cites W1994606458 @default.
- W3033767026 cites W1997564943 @default.
- W3033767026 cites W2006448174 @default.
- W3033767026 cites W2006781415 @default.
- W3033767026 cites W2007970626 @default.
- W3033767026 cites W2013893941 @default.
- W3033767026 cites W2021707161 @default.
- W3033767026 cites W2023813955 @default.
- W3033767026 cites W2027538808 @default.
- W3033767026 cites W2028974055 @default.
- W3033767026 cites W2031806613 @default.
- W3033767026 cites W2042261983 @default.
- W3033767026 cites W2042539224 @default.
- W3033767026 cites W2055025998 @default.
- W3033767026 cites W2055452603 @default.
- W3033767026 cites W2060593560 @default.
- W3033767026 cites W2061551520 @default.
- W3033767026 cites W2063708688 @default.
- W3033767026 cites W2068159141 @default.
- W3033767026 cites W2071786774 @default.
- W3033767026 cites W2073764103 @default.
- W3033767026 cites W2076684935 @default.
- W3033767026 cites W2078800395 @default.
- W3033767026 cites W2091139246 @default.
- W3033767026 cites W2102615476 @default.
- W3033767026 cites W2105952519 @default.
- W3033767026 cites W2111677437 @default.
- W3033767026 cites W2126376370 @default.
- W3033767026 cites W2127378043 @default.
- W3033767026 cites W2128911849 @default.
- W3033767026 cites W2129400521 @default.
- W3033767026 cites W2141935913 @default.
- W3033767026 cites W2144577976 @default.
- W3033767026 cites W2148736202 @default.
- W3033767026 cites W2153086328 @default.
- W3033767026 cites W2160775820 @default.
- W3033767026 cites W2164622044 @default.
- W3033767026 cites W2168437320 @default.
- W3033767026 cites W2176051696 @default.
- W3033767026 cites W2218281080 @default.
- W3033767026 cites W2315561570 @default.
- W3033767026 cites W2316847271 @default.
- W3033767026 cites W2317007499 @default.
- W3033767026 cites W2323493605 @default.
- W3033767026 cites W2324734995 @default.
- W3033767026 cites W2325406720 @default.
- W3033767026 cites W2326201467 @default.
- W3033767026 cites W2329720072 @default.
- W3033767026 cites W2332511416 @default.
- W3033767026 cites W2337851044 @default.
- W3033767026 cites W2403020721 @default.
- W3033767026 cites W2431898019 @default.
- W3033767026 cites W2462480084 @default.
- W3033767026 cites W2560049618 @default.
- W3033767026 cites W2585768892 @default.
- W3033767026 cites W2612535528 @default.
- W3033767026 cites W2613922393 @default.
- W3033767026 cites W2615478152 @default.
- W3033767026 cites W2742483811 @default.
- W3033767026 cites W2771871653 @default.
- W3033767026 cites W2784019437 @default.
- W3033767026 cites W2816524831 @default.
- W3033767026 cites W2867749579 @default.
- W3033767026 cites W2883884104 @default.
- W3033767026 cites W2887426974 @default.
- W3033767026 cites W2892106596 @default.
- W3033767026 cites W2901992810 @default.
- W3033767026 cites W2902954743 @default.
- W3033767026 cites W2946338581 @default.
- W3033767026 cites W2949086505 @default.
- W3033767026 cites W2951589204 @default.
- W3033767026 cites W2996303709 @default.
- W3033767026 cites W3004135483 @default.
- W3033767026 cites W3004459170 @default.
- W3033767026 cites W3008864634 @default.
- W3033767026 cites W634854578 @default.
- W3033767026 doi "https://doi.org/10.1021/acs.orglett.0c01731" @default.