Unique Stereocontrol in Europium(III)-Catalyzed Cyanosilylation of Chiral α-Alkoxy and α-Amino Aldehydes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/21/7/21_7_1169/_pdf
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1. Chiral Lewis acids for enantioselective CC bond formation
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3. The cyclic dipeptide cyclo[(S)-phenylalanyl-(S)-histidyl] as a catalyst for asymmetric addition of hydrogen cyanide to aldehydes
4. Enantioselective autoinduction in the asymmetric hydrocyanation of 3-phenoxybenzaldehyde catalyzed by cyclo[(R)-phenylalanyl-(R)-histidyl]
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1. Protection for the Carbonyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
2. ChemInform Abstract: Unique Stereocontrol in Europium(III)-Catalyzed Cyanosilylation of Chiral α-Alkoxy and α-Amino Aldehydes.;ChemInform;2010-08-20
3. Cyanoesterification of norbornenes catalyzed by palladium: facile synthetic methodology to introduce cyano and ester functionalities via direct carbon–carbon bond cleavage of cyanoformates;Tetrahedron;2006-10
4. P(RNCH2CH2)N: efficient catalysts for the cyanosilylation of aldehydes and ketones;Tetrahedron Letters;2005-11
5. Rare-earth beta-diketonates;Handbook on the Physics and Chemistry of Rare Earths;2005
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