1999
DOI: 10.1002/(sici)1099-0690(199911)1999:11<3127::aid-ejoc3127>3.3.co;2-d
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Chemically Modified -Cyclodextrins as Supramolecular Carriers in the Biphasic Palladium-Catalyzed Cleavage of Allylic Carbonates: Activity Enhancement and Substrate-Selective Catalysis
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“…Finally, it should be noticed that the methylated CDs areas are smaller that those of hydroxypropylated CDs (Table 2 compared entry 1 with entries 2, 3 and 4; compared entry 6 with entries 7 and 8), confirming less hindered structures of methylated CD compared to hydroxypropylated CDs. Although we have reported the efficiency of numerous α-or β-CD derivatives in hydroformylation and Tsuji-Trost reactions [36,42], supplementary catalytic experiments were required to correlate all our surface excess values with catalytic results. Indeed, the effects of DIME-α-CD (10.8), RAME-α-CD (15.0) and CRYSMEB-β-CD (5.0) have never been investigated in the hydroformylation and Tsuji-Trost reactions.…”
Section: Results
mentioning
confidence: 99%
