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0035859352
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A new and general synthetic pathway to strychnos indole alkaloids: Total syntheses of (-)-dehydrotubifoline and (-)-tubifoline by palladium-catalyzed asymmetric allylic substitution
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Mori M, Nakanishi M, Kajishima D, Sato Y (2001) A new and general synthetic pathway to stychnos indole alkaloids: Total syntheses of (+)-dehydrotubifoline and (+)-tubifoline by palladium-catalyzed asymmetric allylic substitution. Org Lett 3:1913-1916 (Pubitemid 33625243)
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Murphy KE, Hoveyda AH (2003) Enantioselective synthesis of a-alkyl-b, g-unsaturated esters through efficient Cu-catalyzed allylic alkylations. J Am Chem Soc 125:4690-4691 (Pubitemid 36505345)
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Synthesis (-D9-trans-tetrahydrocannabinol: Stereocontrol via Mo-catalyzed asymmetric allylic alkylation reaction
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Development of a new and practical route to chiral 3,4-disubstituted cyclopentanones: Asymmetric alkylation and intramolecular cyclopropanation as key C-C bond-forming steps
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Palucki M, Um JM, Yasuda N, Conlon DA, Tsay FR, Hartner FW, Hsiao Y, Marcune B, Karady S, Hughes DL, Dormer PG, Reider PJ (2002) Development of a new and practical route to chiral 3,4-disubstituted cyclopentanones: Asymmetric alkylation and intramolecular cyclopropanation as key C-C bond-forming steps. J Org Chem 67:5508-5516 (Pubitemid 34851590)
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12
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0037021514
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Utilization of molybdenum- and palladium-catayzed dynamic kinetic asymmetric transformations for the preparation of tertiary and quaternary stereogenic centers: A concise synthesis of Tipranavir
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Synthesis of enantiomerically pure (+)-wine lactone based on a palladium-catalyzed enantioselective allylic substitution
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Total synthesis of (α)- and (+)-valienamine via a strategy derived from new palladium-catalyzed reactions
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Gem-diacetates as carbonyl surrogates for asymmetric synthesis. Total syntheses of sphingofungins E and F
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Pd-catalyzed asymmetric allylic alkylation. A short route to the cyclopentyl core of viridenomycin
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18
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A catalytic enantioselective approach to chromans and chomanols. A total synthesis of (-)-calanolides A and B and the vitamin E nucleus [3]
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Enantioselective total synthesis of (+)-galanthamine
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4-Aryloxybutenolides as "chiral aldehyde" equivalents: An efficient enantioselective synthesis of (+)-brefeldin A
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Trost BM, Crawley ML (2002) 4-aryloxybutenolides as "Chiral Aldehyde" equivalents: An efficient enantioselective synthesis of (+)-brefeldin A. J Am Chem Soc 124:9328-9329 (Pubitemid 34856192)
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