Matches in SemOpenAlex for { <https://semopenalex.org/work/W2519700647> ?p ?o ?g. }
- W2519700647 endingPage "9234" @default.
- W2519700647 startingPage "9227" @default.
- W2519700647 abstract "A direct asymmetric Friedel–Crafts (F–C) alkylation reaction between a wide range of indoles and ethyl 2-(4-methoxyphenylimino)acetate catalyzed by Trost’s dinuclear complex is reported. A series of 3-indolylglycine derivatives were synthesized in enantioselectivity of up to >99% enantiomeric excess (ee) using 10 mol% catalyst loading under mild conditions. This atom economic reaction could be run on a gram scale without impacting its enantioselectivity. The absolute stereochemistry of catalytic products was determined by correlation with a known configuration compound. A possible mechanism was proposed for the asymmetric induction." @default.
- W2519700647 created "2016-09-23" @default.
- W2519700647 creator A5004335358 @default.
- W2519700647 creator A5005801799 @default.
- W2519700647 creator A5077803160 @default.
- W2519700647 date "2016-09-27" @default.
- W2519700647 modified "2023-10-17" @default.
- W2519700647 title "Synthesis of 3-Indolylglycine Derivatives via Dinuclear Zinc Catalytic Asymmetric Friedel–Crafts Alkylation Reaction" @default.
- W2519700647 cites W1963766463 @default.
- W2519700647 cites W1970336018 @default.
- W2519700647 cites W1970402643 @default.
- W2519700647 cites W1976562123 @default.
- W2519700647 cites W1976640795 @default.
- W2519700647 cites W1977423095 @default.
- W2519700647 cites W1985446630 @default.
- W2519700647 cites W1985580893 @default.
- W2519700647 cites W1990541497 @default.
- W2519700647 cites W1997644334 @default.
- W2519700647 cites W2002732747 @default.
- W2519700647 cites W2010546696 @default.
- W2519700647 cites W2026094816 @default.
- W2519700647 cites W2027983044 @default.
- W2519700647 cites W2029694100 @default.
- W2519700647 cites W2032828408 @default.
- W2519700647 cites W2034781701 @default.
- W2519700647 cites W2046449834 @default.
- W2519700647 cites W2047776938 @default.
- W2519700647 cites W2049517354 @default.
- W2519700647 cites W2049679247 @default.
- W2519700647 cites W2049979100 @default.
- W2519700647 cites W2052463327 @default.
- W2519700647 cites W2058773066 @default.
- W2519700647 cites W2068164361 @default.
- W2519700647 cites W2081088414 @default.
- W2519700647 cites W2084251109 @default.
- W2519700647 cites W2087683454 @default.
- W2519700647 cites W2089844164 @default.
- W2519700647 cites W2091213218 @default.
- W2519700647 cites W2091621757 @default.
- W2519700647 cites W2099352584 @default.
- W2519700647 cites W2100771494 @default.
- W2519700647 cites W2114885612 @default.
- W2519700647 cites W2120026999 @default.
- W2519700647 cites W2121233306 @default.
- W2519700647 cites W2124764619 @default.
- W2519700647 cites W2128595586 @default.
- W2519700647 cites W2131418393 @default.
- W2519700647 cites W2132802917 @default.
- W2519700647 cites W2143734042 @default.
- W2519700647 cites W2145297283 @default.
- W2519700647 cites W2149663289 @default.
- W2519700647 cites W2159292003 @default.
- W2519700647 cites W2165905697 @default.
- W2519700647 cites W2167798940 @default.
- W2519700647 cites W2171894874 @default.
- W2519700647 cites W2174619953 @default.
- W2519700647 cites W2179339665 @default.
- W2519700647 cites W2179969327 @default.
- W2519700647 cites W2264089796 @default.
- W2519700647 cites W2296175082 @default.
- W2519700647 cites W2316451473 @default.
- W2519700647 cites W2322032591 @default.
- W2519700647 cites W2325311587 @default.
- W2519700647 cites W2329268658 @default.
- W2519700647 cites W2331914710 @default.
- W2519700647 cites W2334167142 @default.
- W2519700647 cites W2334866041 @default.
- W2519700647 cites W2949462260 @default.
- W2519700647 cites W2949618004 @default.
- W2519700647 cites W2949903038 @default.
- W2519700647 cites W2950702012 @default.
- W2519700647 cites W2951583146 @default.
- W2519700647 cites W2951687770 @default.
- W2519700647 cites W2951751079 @default.
- W2519700647 cites W2952289981 @default.
- W2519700647 doi "https://doi.org/10.1021/acs.joc.6b01805" @default.
- W2519700647 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27626632" @default.
- W2519700647 hasPublicationYear "2016" @default.
- W2519700647 type Work @default.
- W2519700647 sameAs 2519700647 @default.
- W2519700647 citedByCount "37" @default.
- W2519700647 countsByYear W25197006472017 @default.
- W2519700647 countsByYear W25197006472018 @default.
- W2519700647 countsByYear W25197006472019 @default.
- W2519700647 countsByYear W25197006472020 @default.
- W2519700647 countsByYear W25197006472021 @default.
- W2519700647 countsByYear W25197006472023 @default.
- W2519700647 crossrefType "journal-article" @default.
- W2519700647 hasAuthorship W2519700647A5004335358 @default.
- W2519700647 hasAuthorship W2519700647A5005801799 @default.
- W2519700647 hasAuthorship W2519700647A5077803160 @default.
- W2519700647 hasConcept C139872579 @default.
- W2519700647 hasConcept C146686406 @default.
- W2519700647 hasConcept C155647269 @default.
- W2519700647 hasConcept C161790260 @default.
- W2519700647 hasConcept C164361826 @default.
- W2519700647 hasConcept C178790620 @default.
- W2519700647 hasConcept C185592680 @default.