Matches in SemOpenAlex for { <https://semopenalex.org/work/W4235983314> ?p ?o ?g. }
- W4235983314 endingPage "9545" @default.
- W4235983314 startingPage "9541" @default.
- W4235983314 abstract "Abstract The first example of a chiral cinchona‐squaramide catalyzed enantioselective intramolecular aza‐Michael addition for the synthesis of dihydroisoquinolines and tetrahydropyridines has been developed. In general, good yields and excellent enantioselctivities were observed. Broad classes of Michael acceptors, such as enones, esters, thioesters, and Weinreb amides, were successful substrates. The possibility of recycling the catalysts has also been demonstrated. An oxidation of combined enamine and keto functionalities on chiral dihydroisoquinolines leads to a single diastereomer of an architecturally unprecedented tetracyclic core without loss in enantioselectivity." @default.
- W4235983314 created "2022-05-12" @default.
- W4235983314 creator A5008150251 @default.
- W4235983314 creator A5031150489 @default.
- W4235983314 creator A5039010928 @default.
- W4235983314 date "2018-06-29" @default.
- W4235983314 modified "2023-10-16" @default.
- W4235983314 title "Cinchonamine Squaramide Catalyzed Asymmetric aza-Michael Reaction: Dihydroisoquinolines and Tetrahydropyridines" @default.
- W4235983314 cites W1965724892 @default.
- W4235983314 cites W1970173055 @default.
- W4235983314 cites W1992927693 @default.
- W4235983314 cites W2003343562 @default.
- W4235983314 cites W2008304599 @default.
- W4235983314 cites W2013959712 @default.
- W4235983314 cites W2015351380 @default.
- W4235983314 cites W2018480674 @default.
- W4235983314 cites W2023508132 @default.
- W4235983314 cites W2024050097 @default.
- W4235983314 cites W2031171691 @default.
- W4235983314 cites W2035497233 @default.
- W4235983314 cites W2041133159 @default.
- W4235983314 cites W2041220500 @default.
- W4235983314 cites W2045933446 @default.
- W4235983314 cites W2046171430 @default.
- W4235983314 cites W2049084706 @default.
- W4235983314 cites W2050261344 @default.
- W4235983314 cites W2051229074 @default.
- W4235983314 cites W2052614607 @default.
- W4235983314 cites W2053634767 @default.
- W4235983314 cites W2054376935 @default.
- W4235983314 cites W2057492990 @default.
- W4235983314 cites W2058007531 @default.
- W4235983314 cites W2061598420 @default.
- W4235983314 cites W2061802342 @default.
- W4235983314 cites W2062590568 @default.
- W4235983314 cites W2063700634 @default.
- W4235983314 cites W2065056504 @default.
- W4235983314 cites W2079568090 @default.
- W4235983314 cites W2080487333 @default.
- W4235983314 cites W2081190477 @default.
- W4235983314 cites W2084342072 @default.
- W4235983314 cites W2086744748 @default.
- W4235983314 cites W2095595702 @default.
- W4235983314 cites W2117169305 @default.
- W4235983314 cites W2117275296 @default.
- W4235983314 cites W2120466333 @default.
- W4235983314 cites W2122818458 @default.
- W4235983314 cites W2125333006 @default.
- W4235983314 cites W2145184530 @default.
- W4235983314 cites W2151752727 @default.
- W4235983314 cites W2157265137 @default.
- W4235983314 cites W2159216169 @default.
- W4235983314 cites W2163846856 @default.
- W4235983314 cites W2164203810 @default.
- W4235983314 cites W2269747418 @default.
- W4235983314 cites W2280200208 @default.
- W4235983314 cites W2292085686 @default.
- W4235983314 cites W2317561833 @default.
- W4235983314 cites W2322826824 @default.
- W4235983314 cites W2334363680 @default.
- W4235983314 cites W2372212411 @default.
- W4235983314 cites W2388434347 @default.
- W4235983314 cites W2411052289 @default.
- W4235983314 cites W2460708209 @default.
- W4235983314 cites W2523633622 @default.
- W4235983314 cites W2547070825 @default.
- W4235983314 cites W2554893025 @default.
- W4235983314 cites W2580807745 @default.
- W4235983314 cites W2618214716 @default.
- W4235983314 cites W2696186415 @default.
- W4235983314 cites W2751087354 @default.
- W4235983314 cites W2950544573 @default.
- W4235983314 cites W2952380974 @default.
- W4235983314 cites W2952773184 @default.
- W4235983314 cites W2953284536 @default.
- W4235983314 cites W4233199574 @default.
- W4235983314 cites W4234432235 @default.
- W4235983314 cites W4244116565 @default.
- W4235983314 cites W4244847871 @default.
- W4235983314 cites W4249962414 @default.
- W4235983314 cites W4252552687 @default.
- W4235983314 cites W4253693569 @default.
- W4235983314 cites W4253919997 @default.
- W4235983314 doi "https://doi.org/10.1002/ange.201805020" @default.
- W4235983314 hasPublicationYear "2018" @default.
- W4235983314 type Work @default.
- W4235983314 citedByCount "5" @default.
- W4235983314 countsByYear W42359833142018 @default.
- W4235983314 countsByYear W42359833142020 @default.
- W4235983314 countsByYear W42359833142023 @default.
- W4235983314 crossrefType "journal-article" @default.
- W4235983314 hasAuthorship W4235983314A5008150251 @default.
- W4235983314 hasAuthorship W4235983314A5031150489 @default.
- W4235983314 hasAuthorship W4235983314A5039010928 @default.
- W4235983314 hasConcept C112423150 @default.
- W4235983314 hasConcept C138716334 @default.
- W4235983314 hasConcept C146686406 @default.
- W4235983314 hasConcept C161790260 @default.