Matches in SemOpenAlex for { <https://semopenalex.org/work/W2003269718> ?p ?o ?g. }
- W2003269718 endingPage "379" @default.
- W2003269718 startingPage "366" @default.
- W2003269718 abstract "Abstract Phosphane‐free Pd 0 ‐catalyzed intramolecular aromatic amination was studied. o ‐Halophenethylamines and 3‐( o ‐halophenyl)propylamines were found to be transformed into indolines and quinolines in a catalytic system based on Pd(OAc) 2 and Cu(OAc) 2 in the presence of K 2 CO 3 . Application of the method to substrates containing isoquinoline rings – the 1‐( o ‐bromobenzyl)‐3,4‐dihydroisoquinolines 6 , the 1‐( o ‐bromobenzyl)‐1,2,3,4‐tetrahydroisoquinolines 7 , and the 1‐( o ‐bromophenethyl)isoquinolines 9 – provided the indolo[2,1‐ a ]isoquinoline and dibenzo[ a,f ]quinolizine ring systems 8 and 10 . Extension of the method to β‐carbolines (compounds 11 , 12 , and 17 ) produced the benz[ f ]indolo[2,3‐ a ]indolizine‐13‐ones 15 and the benz[ f ]indolo[2,3‐ a ]quinolizine 18 . The benzo[ f ]pyrido[3,4‐ a ]indolizine and indolo[ f ]pyrido[3,4‐ a ]indolizin‐12‐one ring systems 27 and 31 were built in a similar manner. It was also found that under an atmosphere of CO the same catalytic system produced the corresponding benzolactams, the isoquino[2,1‐ a ][2,7]naphthyridine 34 and the indolo[2,3‐ a ]pyrido[ g ]quinolizin‐8‐one 36 [(±)‐dihydronaucléfine] in good yields." @default.
- W2003269718 created "2016-06-24" @default.
- W2003269718 creator A5014046257 @default.
- W2003269718 creator A5020828255 @default.
- W2003269718 creator A5023896161 @default.
- W2003269718 creator A5027425660 @default.
- W2003269718 creator A5036574972 @default.
- W2003269718 creator A5059802624 @default.
- W2003269718 creator A5064243487 @default.
- W2003269718 creator A5066419790 @default.
- W2003269718 creator A5071461622 @default.
- W2003269718 date "2011-11-17" @default.
- W2003269718 modified "2023-10-12" @default.
- W2003269718 title "Phosphane-Free Pd0-Catalyzed Cycloamination and Carbonylation with Pd(OAc)2 and Cu(OAc)2 in the Presence of K2CO3: Preparation of Benzocyclic Amines and Benzolactams" @default.
- W2003269718 cites W102477270 @default.
- W2003269718 cites W1508919460 @default.
- W2003269718 cites W1526844500 @default.
- W2003269718 cites W1573640834 @default.
- W2003269718 cites W1582532363 @default.
- W2003269718 cites W1963712369 @default.
- W2003269718 cites W1963934721 @default.
- W2003269718 cites W1964044315 @default.
- W2003269718 cites W1966101368 @default.
- W2003269718 cites W1968649837 @default.
- W2003269718 cites W1968722611 @default.
- W2003269718 cites W1969968017 @default.
- W2003269718 cites W1970063365 @default.
- W2003269718 cites W1971009269 @default.
- W2003269718 cites W1973422955 @default.
- W2003269718 cites W1973955987 @default.
- W2003269718 cites W1974193852 @default.
- W2003269718 cites W1975687793 @default.
- W2003269718 cites W1976767241 @default.
- W2003269718 cites W1977202605 @default.
- W2003269718 cites W1979135049 @default.
- W2003269718 cites W1979489398 @default.
- W2003269718 cites W1979578538 @default.
- W2003269718 cites W1979703254 @default.
- W2003269718 cites W1980445753 @default.
- W2003269718 cites W1981812077 @default.
- W2003269718 cites W1982768703 @default.
- W2003269718 cites W1984314768 @default.
- W2003269718 cites W1984353914 @default.
- W2003269718 cites W1985376680 @default.
- W2003269718 cites W1985414587 @default.
- W2003269718 cites W1985795397 @default.
- W2003269718 cites W1987860184 @default.
- W2003269718 cites W1989484868 @default.
- W2003269718 cites W1990103879 @default.
- W2003269718 cites W1990187247 @default.
- W2003269718 cites W1990732631 @default.
- W2003269718 cites W1991436717 @default.
- W2003269718 cites W1991906913 @default.
- W2003269718 cites W1991927619 @default.
- W2003269718 cites W1991965792 @default.
- W2003269718 cites W1993649816 @default.
- W2003269718 cites W1993730602 @default.
- W2003269718 cites W1994102996 @default.
- W2003269718 cites W1998870115 @default.
- W2003269718 cites W1999132406 @default.
- W2003269718 cites W1999906396 @default.
- W2003269718 cites W2001199429 @default.
- W2003269718 cites W2004519134 @default.
- W2003269718 cites W2007355031 @default.
- W2003269718 cites W2008217595 @default.
- W2003269718 cites W2008244783 @default.
- W2003269718 cites W2008394094 @default.
- W2003269718 cites W2008601612 @default.
- W2003269718 cites W2010587610 @default.
- W2003269718 cites W2011591036 @default.
- W2003269718 cites W2012057029 @default.
- W2003269718 cites W2014240385 @default.
- W2003269718 cites W2014944527 @default.
- W2003269718 cites W2016757577 @default.
- W2003269718 cites W2018825486 @default.
- W2003269718 cites W2018857076 @default.
- W2003269718 cites W2020920139 @default.
- W2003269718 cites W2021021033 @default.
- W2003269718 cites W2021737900 @default.
- W2003269718 cites W2022625478 @default.
- W2003269718 cites W2023261919 @default.
- W2003269718 cites W2024098876 @default.
- W2003269718 cites W2024442047 @default.
- W2003269718 cites W2025781186 @default.
- W2003269718 cites W2026149308 @default.
- W2003269718 cites W2026210088 @default.
- W2003269718 cites W2026832749 @default.
- W2003269718 cites W2030173073 @default.
- W2003269718 cites W2031255003 @default.
- W2003269718 cites W2032014061 @default.
- W2003269718 cites W2033716597 @default.
- W2003269718 cites W2039167778 @default.
- W2003269718 cites W2041515292 @default.
- W2003269718 cites W2042515452 @default.
- W2003269718 cites W2042653815 @default.
- W2003269718 cites W2043079728 @default.
- W2003269718 cites W2043666473 @default.
- W2003269718 cites W2043889031 @default.