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Volumn 59, Issue 1, 2011, Pages 1-22

Development of atom-economical catalytic asymmetric reactions under proton transfer conditions: Construction of tetrasubstituted stereogenic centers and their application to therapeutics

Author keywords

Asymmetric catalysis; Atom economy; Proton transfer; Rare earth metal; Tetrasubstituted stereogenic center

Indexed keywords

1,2 DICARBONYL DERIVATIVE; ALDOSE REDUCTASE INHIBITOR; ALKENE DERIVATIVE; ALLYL COMPOUND; ALPHA AMINO ACID; BENZALDEHYDE; BETA 3 ADRENERGIC RECEPTOR STIMULATING AGENT; BRONSTED ACID; CARBONYL DERIVATIVE; CHLOROFORM; CINCHONIDINE; CYANOKETONE; DEFERASIROX; DICHLOROMETHANE; DIMETHYL SULFOXIDE; ETHANE; ISOBUTYRALDEHYDE; LEWIS ACID; METHANOL; MONOBENZONE; N,N DIMETHYLACETAMIDE; NITROALKANE; PIPERIDINE DERIVATIVE; PROTON; RANIRESTAT; SOLVENT; SUCCINIMIDE DERIVATIVE; TETRAHYDROFURAN; THIOAMIDE; UNINDEXED DRUG;

EID: 78650849014     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.59.1     Document Type: Review
Times cited : (19)

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    • For direct catalytic asymmetric aldol (-type) reactions using aldol donors in the carboxylic acid oxidation state without electron-withdrawing α-substituents: alkylnitriles (up to 77% ee), see: Suto Y., Tsuji R., Kanai M., Shibasaki M., Org. Lett., 7, 3757-3760 (2005).
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    • For direct catalytic asymmetric aldol (-type) reactions using aldol donors in the carboxylic acid oxidation state without electron-withdrawing α-substituents: activated amides (up to 33% ee), see: Saito S., Kobayashi S., J. Am. Chem. Soc., 128, 8704-8705 (2006).
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