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- W3013122421 endingPage "2780" @default.
- W3013122421 startingPage "2771" @default.
- W3013122421 abstract "An efficient and protecting‐group‐directed highly diastereoselective (≥ 99:1) synthesis of tetrahydro‐3 H ‐pyrrolo[ 2,3 ‐ c ]quinolines bearing four contiguous chiral centers was achieved by using intermolecular Michael addition followed by intramolecular Mannich cyclization strategy. The domino reaction proceeded well with a broad scope of substrates under mild conditions and afforded the corresponding products in good to excellent yields. The synthetic protocol provided a straightforward synthetic route to tetrahydropyrroloquinolines as single diastereomers, which are difficult to synthesize by other methodologies." @default.
- W3013122421 created "2020-04-03" @default.
- W3013122421 creator A5000184114 @default.
- W3013122421 creator A5006284460 @default.
- W3013122421 creator A5019975675 @default.
- W3013122421 creator A5023891849 @default.
- W3013122421 creator A5035230211 @default.
- W3013122421 date "2020-04-30" @default.
- W3013122421 modified "2023-09-27" @default.
- W3013122421 title "Protecting-Group-Directed Diastereoselective Synthesis of Substituted Tetrahydropyrroloquinolines" @default.
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- W3013122421 cites W1969380258 @default.
- W3013122421 cites W1972928954 @default.
- W3013122421 cites W1973651288 @default.
- W3013122421 cites W1975520800 @default.
- W3013122421 cites W1980972289 @default.
- W3013122421 cites W1982907022 @default.
- W3013122421 cites W1983806218 @default.
- W3013122421 cites W1984393702 @default.
- W3013122421 cites W1986952886 @default.
- W3013122421 cites W1988205318 @default.
- W3013122421 cites W1991700978 @default.
- W3013122421 cites W1992100801 @default.
- W3013122421 cites W1992848154 @default.
- W3013122421 cites W1995141707 @default.
- W3013122421 cites W2014007912 @default.
- W3013122421 cites W2016411123 @default.
- W3013122421 cites W2017975542 @default.
- W3013122421 cites W2018823912 @default.
- W3013122421 cites W2019710602 @default.
- W3013122421 cites W2026076442 @default.
- W3013122421 cites W2026223922 @default.
- W3013122421 cites W2028935067 @default.
- W3013122421 cites W2031239668 @default.
- W3013122421 cites W2034176914 @default.
- W3013122421 cites W2037277012 @default.
- W3013122421 cites W2040351631 @default.
- W3013122421 cites W2052402888 @default.
- W3013122421 cites W2057102390 @default.
- W3013122421 cites W2066404668 @default.
- W3013122421 cites W2067887135 @default.
- W3013122421 cites W2070921346 @default.
- W3013122421 cites W2072397144 @default.
- W3013122421 cites W2074899890 @default.
- W3013122421 cites W2075572227 @default.
- W3013122421 cites W2077074100 @default.
- W3013122421 cites W2077555850 @default.
- W3013122421 cites W2079722025 @default.
- W3013122421 cites W2106005544 @default.
- W3013122421 cites W2113532458 @default.
- W3013122421 cites W2118180102 @default.
- W3013122421 cites W2119050116 @default.
- W3013122421 cites W2122592786 @default.
- W3013122421 cites W2131138952 @default.
- W3013122421 cites W2134764589 @default.
- W3013122421 cites W2143976767 @default.
- W3013122421 cites W2144417580 @default.
- W3013122421 cites W2145521507 @default.
- W3013122421 cites W2151636659 @default.
- W3013122421 cites W2151977774 @default.
- W3013122421 cites W2158614544 @default.
- W3013122421 cites W2163058448 @default.
- W3013122421 cites W2170255604 @default.
- W3013122421 cites W2170609373 @default.
- W3013122421 cites W2182300373 @default.
- W3013122421 cites W2281948879 @default.
- W3013122421 cites W2313103067 @default.
- W3013122421 cites W2317875130 @default.
- W3013122421 cites W2318906785 @default.
- W3013122421 cites W2324566582 @default.
- W3013122421 cites W2331740084 @default.
- W3013122421 cites W2342434776 @default.
- W3013122421 cites W2468333613 @default.
- W3013122421 cites W2500772578 @default.
- W3013122421 cites W2592152985 @default.
- W3013122421 cites W2783298288 @default.
- W3013122421 cites W2789217565 @default.
- W3013122421 cites W2802316497 @default.
- W3013122421 cites W2898790346 @default.
- W3013122421 cites W2902867023 @default.
- W3013122421 cites W2917314516 @default.
- W3013122421 cites W2938995977 @default.
- W3013122421 cites W2940159625 @default.
- W3013122421 cites W2948875664 @default.
- W3013122421 cites W2949267973 @default.
- W3013122421 cites W2949707394 @default.
- W3013122421 cites W2951054868 @default.
- W3013122421 cites W2967280271 @default.
- W3013122421 cites W4229790567 @default.
- W3013122421 cites W4236941167 @default.
- W3013122421 cites W4242060636 @default.
- W3013122421 cites W4246338290 @default.
- W3013122421 cites W4249065849 @default.
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- W3013122421 doi "https://doi.org/10.1002/ejoc.202000348" @default.
- W3013122421 hasPublicationYear "2020" @default.
- W3013122421 type Work @default.