Matches in SemOpenAlex for { <https://semopenalex.org/work/W2950409526> ?p ?o ?g. }
- W2950409526 endingPage "73" @default.
- W2950409526 startingPage "63" @default.
- W2950409526 abstract "The first catalytic asymmetric hetero-Diels–Alder (HDA) reaction between 3-tert-butyldimethylsilyloxy-1-dimethylamino-1,3-pentadiene (4-methyl-substituted Rawal’s diene) and aldehydes is described. With 3 mol % of dirhodium(II) tetrakis[N-benzene-fused-phthaloyl-(S)-piperidinonate], Rh2((S)-BPTPI)4, the cycloaddition reaction proceeded exclusively in an endo fashion and gave, after a novel sequential treatment with dimethyl acetylenedicarboxylate and acetyl chloride, the corresponding 2,3-cis-disubstituted dihydropyranones with up to 98% ee and perfect diastereoselectivity. The utility of this catalytic protocol was demonstrated by an asymmetric synthesis of the (−)-cis-aerangis lactone." @default.
- W2950409526 created "2019-06-27" @default.
- W2950409526 creator A5008797071 @default.
- W2950409526 creator A5019647047 @default.
- W2950409526 creator A5023045493 @default.
- W2950409526 creator A5035363703 @default.
- W2950409526 date "2014-01-01" @default.
- W2950409526 modified "2023-09-23" @default.
- W2950409526 title "Enantio- and diastereoselective hetero-Diels–Alder reactions between 4-methyl-substituted Rawal’s diene and aldehydes catalyzed by chiral dirhodium(II) carboxamidates: catalytic asymmetric synthesis of (−)-cis-aerangis lactone" @default.
- W2950409526 cites W1541803153 @default.
- W2950409526 cites W1662538545 @default.
- W2950409526 cites W1969511041 @default.
- W2950409526 cites W1971859928 @default.
- W2950409526 cites W1976165583 @default.
- W2950409526 cites W1976400949 @default.
- W2950409526 cites W1977157431 @default.
- W2950409526 cites W1977264850 @default.
- W2950409526 cites W1978928926 @default.
- W2950409526 cites W1979513828 @default.
- W2950409526 cites W1981887963 @default.
- W2950409526 cites W1983791194 @default.
- W2950409526 cites W1985957111 @default.
- W2950409526 cites W1988156143 @default.
- W2950409526 cites W1991127819 @default.
- W2950409526 cites W1993800646 @default.
- W2950409526 cites W1993888371 @default.
- W2950409526 cites W1994533618 @default.
- W2950409526 cites W1998305107 @default.
- W2950409526 cites W1998384499 @default.
- W2950409526 cites W1999235865 @default.
- W2950409526 cites W1999513405 @default.
- W2950409526 cites W2004866081 @default.
- W2950409526 cites W2008651293 @default.
- W2950409526 cites W2009537490 @default.
- W2950409526 cites W2010265126 @default.
- W2950409526 cites W2010967803 @default.
- W2950409526 cites W2019238755 @default.
- W2950409526 cites W2020452933 @default.
- W2950409526 cites W2024133447 @default.
- W2950409526 cites W2027535420 @default.
- W2950409526 cites W2032698433 @default.
- W2950409526 cites W2036879289 @default.
- W2950409526 cites W2044964964 @default.
- W2950409526 cites W2046680132 @default.
- W2950409526 cites W2049711298 @default.
- W2950409526 cites W2054282091 @default.
- W2950409526 cites W2063688160 @default.
- W2950409526 cites W2063799349 @default.
- W2950409526 cites W2065024376 @default.
- W2950409526 cites W2067656108 @default.
- W2950409526 cites W2072654506 @default.
- W2950409526 cites W2081517259 @default.
- W2950409526 cites W2086096868 @default.
- W2950409526 cites W2091726474 @default.
- W2950409526 cites W2092180848 @default.
- W2950409526 cites W2093734407 @default.
- W2950409526 cites W2094024901 @default.
- W2950409526 cites W2107393483 @default.
- W2950409526 cites W2123514276 @default.
- W2950409526 cites W2134200842 @default.
- W2950409526 cites W2140815811 @default.
- W2950409526 cites W2141050098 @default.
- W2950409526 cites W2146862011 @default.
- W2950409526 cites W2148830666 @default.
- W2950409526 cites W2153721661 @default.
- W2950409526 cites W2155381532 @default.
- W2950409526 cites W2161628155 @default.
- W2950409526 cites W2166421534 @default.
- W2950409526 cites W2167568255 @default.
- W2950409526 cites W2175261023 @default.
- W2950409526 cites W2176125203 @default.
- W2950409526 cites W2325398662 @default.
- W2950409526 cites W2330733209 @default.
- W2950409526 cites W2949137942 @default.
- W2950409526 cites W2949163087 @default.
- W2950409526 cites W2949414229 @default.
- W2950409526 cites W2949438036 @default.
- W2950409526 cites W2950127080 @default.
- W2950409526 cites W2950806884 @default.
- W2950409526 cites W2951106892 @default.
- W2950409526 cites W2951169682 @default.
- W2950409526 cites W2951196206 @default.
- W2950409526 cites W2951533758 @default.
- W2950409526 cites W2951943414 @default.
- W2950409526 cites W2951961569 @default.
- W2950409526 cites W2952467430 @default.
- W2950409526 cites W2953031451 @default.
- W2950409526 cites W2953109906 @default.
- W2950409526 cites W2953124863 @default.
- W2950409526 cites W3004533299 @default.
- W2950409526 cites W4253551565 @default.
- W2950409526 doi "https://doi.org/10.1016/j.tetasy.2013.10.016" @default.
- W2950409526 hasPublicationYear "2014" @default.
- W2950409526 type Work @default.
- W2950409526 sameAs 2950409526 @default.
- W2950409526 citedByCount "17" @default.
- W2950409526 countsByYear W29504095262014 @default.
- W2950409526 countsByYear W29504095262015 @default.