Matches in SemOpenAlex for { <https://semopenalex.org/work/W2734242256> ?p ?o ?g. }
- W2734242256 endingPage "7938" @default.
- W2734242256 startingPage "7920" @default.
- W2734242256 abstract "Diverse general high-yield routes for novel thieno-fused five- and six-membered nitrogen and oxygen heterocycles such as thieno[3,2-b]pyrroles, thieno[3,2-b]furans, thieno[3,2-b]indoles, thieno[3,2-b]benzofurans, thieno[3,2-b]pyridine-5-ones, thieno[3,2-b]pyran-5-ones, thieno[3,2-b]isoquinolin-5-ones, thieno[3,2-b]chromen-5-ones, thieno[3,2-b]quinolin-9-ones, and thieno[3,2-b]chromen-9-ones have been developed via in situ or stepwise intramolecular heteroannulation of newly synthesized 4,5-substituted 3-amino- or 3-hydroxy 2-functionalized thiophenes. These substituted 3-amino/hydroxythiophenes were readily obtained in high yields from easily accessible precursors, in a sequential one-pot process, by treatment of a range of (het)aryl/unsubstituted acetonitriles or acetates with (het)aryl dithioesters in the presence of LDA, followed by in situ alkylation–intramolecular condensation of the resulting enethiolate salts with functionalized activated methylene halides. The functionalized activated methylene halides employed in these reactions for the synthesis of various thieno-fused heterocycles were cinnamyl bromide, 2-bromobenzyl chloride, bromocrotonate, 2-(bromomethyl)benzoate, and 2-chlorophenacyl bromide. A few of the 4,5-substituted 3-amino/hydroxy-2-stryrylthiophenes (or 2-acrylates) displayed strong fluorescence, and their absorption/emission spectra have also been examined." @default.
- W2734242256 created "2017-07-14" @default.
- W2734242256 creator A5001214378 @default.
- W2734242256 creator A5044746087 @default.
- W2734242256 creator A5087938002 @default.
- W2734242256 date "2017-07-18" @default.
- W2734242256 modified "2023-10-18" @default.
- W2734242256 title "Synthesis of Thieno-Fused Five- and Six-Membered Nitrogen and Oxygen Heterocycles via Intramolecular Heteroannulation of 4,5-Substituted 3-Amino or 3-Hydroxy 2-Functionalized Thiophenes" @default.
- W2734242256 cites W154038249 @default.
- W2734242256 cites W1551925748 @default.
- W2734242256 cites W1974774522 @default.
- W2734242256 cites W1976861561 @default.
- W2734242256 cites W1977322978 @default.
- W2734242256 cites W1978082033 @default.
- W2734242256 cites W1982462327 @default.
- W2734242256 cites W1985995672 @default.
- W2734242256 cites W1987606761 @default.
- W2734242256 cites W1993541016 @default.
- W2734242256 cites W1996966747 @default.
- W2734242256 cites W1997395077 @default.
- W2734242256 cites W1997770703 @default.
- W2734242256 cites W2001052740 @default.
- W2734242256 cites W2001995589 @default.
- W2734242256 cites W2003731708 @default.
- W2734242256 cites W2010101793 @default.
- W2734242256 cites W2017095161 @default.
- W2734242256 cites W2018655403 @default.
- W2734242256 cites W2024558403 @default.
- W2734242256 cites W2025161945 @default.
- W2734242256 cites W2025297417 @default.
- W2734242256 cites W2031522001 @default.
- W2734242256 cites W2032275673 @default.
- W2734242256 cites W2036211009 @default.
- W2734242256 cites W2036990896 @default.
- W2734242256 cites W2042782692 @default.
- W2734242256 cites W2059197962 @default.
- W2734242256 cites W2060689359 @default.
- W2734242256 cites W2061705443 @default.
- W2734242256 cites W2064278512 @default.
- W2734242256 cites W2065760185 @default.
- W2734242256 cites W2065889803 @default.
- W2734242256 cites W2066319332 @default.
- W2734242256 cites W2067040862 @default.
- W2734242256 cites W2075073048 @default.
- W2734242256 cites W2078844308 @default.
- W2734242256 cites W2082254162 @default.
- W2734242256 cites W2082558575 @default.
- W2734242256 cites W2082881448 @default.
- W2734242256 cites W2085182569 @default.
- W2734242256 cites W2085313140 @default.
- W2734242256 cites W2087272850 @default.
- W2734242256 cites W2088086939 @default.
- W2734242256 cites W2088701078 @default.
- W2734242256 cites W2090517202 @default.
- W2734242256 cites W2092033067 @default.
- W2734242256 cites W2092203122 @default.
- W2734242256 cites W2098693239 @default.
- W2734242256 cites W2100268373 @default.
- W2734242256 cites W2100687244 @default.
- W2734242256 cites W2100996921 @default.
- W2734242256 cites W2107479708 @default.
- W2734242256 cites W2122786921 @default.
- W2734242256 cites W2124067928 @default.
- W2734242256 cites W2131699263 @default.
- W2734242256 cites W2134720566 @default.
- W2734242256 cites W2140247121 @default.
- W2734242256 cites W2140367837 @default.
- W2734242256 cites W2140871226 @default.
- W2734242256 cites W2141326037 @default.
- W2734242256 cites W2148035249 @default.
- W2734242256 cites W2149724205 @default.
- W2734242256 cites W2160046988 @default.
- W2734242256 cites W2163771010 @default.
- W2734242256 cites W2174537078 @default.
- W2734242256 cites W2180807935 @default.
- W2734242256 cites W2201190100 @default.
- W2734242256 cites W2230967888 @default.
- W2734242256 cites W2269259439 @default.
- W2734242256 cites W2314018283 @default.
- W2734242256 cites W2314471496 @default.
- W2734242256 cites W2317821468 @default.
- W2734242256 cites W2321514056 @default.
- W2734242256 cites W2322135194 @default.
- W2734242256 cites W2326170401 @default.
- W2734242256 cites W2328714476 @default.
- W2734242256 cites W2400668396 @default.
- W2734242256 cites W2464595708 @default.
- W2734242256 cites W2597242996 @default.
- W2734242256 cites W2949143071 @default.
- W2734242256 cites W2949490815 @default.
- W2734242256 cites W2950459472 @default.
- W2734242256 cites W2950568676 @default.
- W2734242256 cites W2950893917 @default.
- W2734242256 cites W2951204249 @default.
- W2734242256 cites W2952248377 @default.
- W2734242256 cites W2952435520 @default.
- W2734242256 cites W2953210974 @default.
- W2734242256 cites W2953220485 @default.