Matches in SemOpenAlex for { <https://semopenalex.org/work/W2946828112> ?p ?o ?g. }
- W2946828112 endingPage "3569" @default.
- W2946828112 startingPage "3553" @default.
- W2946828112 abstract "The reductive coupling of cyclic imides and ω-amidoesters with benzophenones by Zn-TiCl4 in THF and subsequent acid-catalyzed dehydration gave 5-diarylmethylene-1,5-dihydropyrrol-2-ones A, 6-diarylmethyl-2-pyridones B, and ω-(diarylmethylene)lactams C. In a similar manner, 3-((benzyloxy)carbonyl)amino substituted A, B, and C were synthesized from the corresponding 3-((benzyloxy)carbonyl)amino cyclic imides and ω-((benzyloxy)carbonyl)amino-ω-amidoesters prepared from L-aspartic and L-glutamic acids. In addition, 4- and 5-((benzyloxy)carbonyl)amino substituted C were also obtained by the same procedures from 2-((benzyloxy)carbonyl)amino-ω-amidoesters prepared from L-asparagine and L-glutamine, respectively." @default.
- W2946828112 created "2019-05-29" @default.
- W2946828112 creator A5001208211 @default.
- W2946828112 creator A5020938638 @default.
- W2946828112 creator A5091082512 @default.
- W2946828112 date "2019-06-01" @default.
- W2946828112 modified "2023-10-02" @default.
- W2946828112 title "Reductive coupling of aliphatic cyclic imides and ω-amidoesters with benzophenones by low-valent titanium: Synthesis of 5-diarylmethylene-1,5-dihydropyrrol-2-ones, 6-diarylmethyl-2-pyridones, and ω-(diarylmethylene)lactams" @default.
- W2946828112 cites W1969479808 @default.
- W2946828112 cites W1970695365 @default.
- W2946828112 cites W1973601085 @default.
- W2946828112 cites W1981861883 @default.
- W2946828112 cites W1984302936 @default.
- W2946828112 cites W1984733142 @default.
- W2946828112 cites W1994113726 @default.
- W2946828112 cites W1995446227 @default.
- W2946828112 cites W1999836355 @default.
- W2946828112 cites W2001173520 @default.
- W2946828112 cites W2002290130 @default.
- W2946828112 cites W2009367929 @default.
- W2946828112 cites W2040897726 @default.
- W2946828112 cites W2049016983 @default.
- W2946828112 cites W2049118547 @default.
- W2946828112 cites W2050296291 @default.
- W2946828112 cites W2056840911 @default.
- W2946828112 cites W2057209132 @default.
- W2946828112 cites W2065619364 @default.
- W2946828112 cites W2069410927 @default.
- W2946828112 cites W2075943579 @default.
- W2946828112 cites W2086747002 @default.
- W2946828112 cites W2118676236 @default.
- W2946828112 cites W2170623768 @default.
- W2946828112 cites W2179905051 @default.
- W2946828112 cites W2193668187 @default.
- W2946828112 cites W2201474671 @default.
- W2946828112 cites W2296595939 @default.
- W2946828112 cites W2319067779 @default.
- W2946828112 cites W2321973402 @default.
- W2946828112 cites W2340610485 @default.
- W2946828112 cites W2397539806 @default.
- W2946828112 cites W2475178448 @default.
- W2946828112 cites W2512543693 @default.
- W2946828112 cites W2577926200 @default.
- W2946828112 cites W2764214258 @default.
- W2946828112 cites W2770307810 @default.
- W2946828112 cites W2789530022 @default.
- W2946828112 cites W2791394337 @default.
- W2946828112 cites W2949383734 @default.
- W2946828112 cites W2949926463 @default.
- W2946828112 cites W2950073764 @default.
- W2946828112 cites W2950407142 @default.
- W2946828112 cites W2951766148 @default.
- W2946828112 cites W4253637974 @default.
- W2946828112 cites W995400036 @default.
- W2946828112 doi "https://doi.org/10.1016/j.tet.2019.05.013" @default.
- W2946828112 hasPublicationYear "2019" @default.
- W2946828112 type Work @default.
- W2946828112 sameAs 2946828112 @default.
- W2946828112 citedByCount "4" @default.
- W2946828112 countsByYear W29468281122020 @default.
- W2946828112 countsByYear W29468281122021 @default.
- W2946828112 countsByYear W29468281122022 @default.
- W2946828112 countsByYear W29468281122023 @default.
- W2946828112 crossrefType "journal-article" @default.
- W2946828112 hasAuthorship W2946828112A5001208211 @default.
- W2946828112 hasAuthorship W2946828112A5020938638 @default.
- W2946828112 hasAuthorship W2946828112A5091082512 @default.
- W2946828112 hasConcept C155647269 @default.
- W2946828112 hasConcept C161790260 @default.
- W2946828112 hasConcept C178790620 @default.
- W2946828112 hasConcept C185592680 @default.
- W2946828112 hasConcept C2775895851 @default.
- W2946828112 hasConcept C2777247709 @default.
- W2946828112 hasConcept C2779349466 @default.
- W2946828112 hasConcept C515207424 @default.
- W2946828112 hasConcept C55493867 @default.
- W2946828112 hasConcept C71240020 @default.
- W2946828112 hasConceptScore W2946828112C155647269 @default.
- W2946828112 hasConceptScore W2946828112C161790260 @default.
- W2946828112 hasConceptScore W2946828112C178790620 @default.
- W2946828112 hasConceptScore W2946828112C185592680 @default.
- W2946828112 hasConceptScore W2946828112C2775895851 @default.
- W2946828112 hasConceptScore W2946828112C2777247709 @default.
- W2946828112 hasConceptScore W2946828112C2779349466 @default.
- W2946828112 hasConceptScore W2946828112C515207424 @default.
- W2946828112 hasConceptScore W2946828112C55493867 @default.
- W2946828112 hasConceptScore W2946828112C71240020 @default.
- W2946828112 hasIssue "26" @default.
- W2946828112 hasLocation W29468281121 @default.
- W2946828112 hasOpenAccess W2946828112 @default.
- W2946828112 hasPrimaryLocation W29468281121 @default.
- W2946828112 hasRelatedWork W1966399229 @default.
- W2946828112 hasRelatedWork W1976668673 @default.
- W2946828112 hasRelatedWork W2003466182 @default.
- W2946828112 hasRelatedWork W2010767342 @default.
- W2946828112 hasRelatedWork W2053957235 @default.
- W2946828112 hasRelatedWork W2070274699 @default.
- W2946828112 hasRelatedWork W2110644991 @default.