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ChemInform Abstract: A New Asymmetric Synthesis of (S)-Dolaphenine and Its Heteroaromatic Congeners Utilizing (+)-2-Hydroxy-3-pinanone and (-)-3-Hydroxy-2- caranone as Chiral Auxiliaries.

✍ Scribed by N. IRAKO; Y. HAMADA; T. SHIOIRI

Book ID: 112029048
Publisher: John Wiley and Sons
Year: 2010
Weight: 34 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199611245

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📜 SIMILAR VOLUMES

ChemInform Abstract: Computational Studi

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ChemInform Abstract: (R)- and (S)-3-Hydr

ChemInform Abstract: (R)- and (S)-3-Hydroxy-4,4-dimethyl-1-phenyl-2-pyrrolidinone as Chiral Auxiliaries for the Asymmetric Synthesis of α-Hydroxy Acids.

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ChemInform Abstract: (S)-2-(Dibenzylamin

ChemInform Abstract: (S)-2-(Dibenzylamino)-3-phenylpropanal as a Chiral Auxiliary: A New Strategy for the Asymmetric Synthesis of 2-Substituted Alcohols.

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1998 alcohols alcohols (acyclic compounds) P 0110 33 -116 (S)-2-(Dibenzylamino)-3-phenylpropanal as a Chiral Auxiliary: A New Strategy for the Asymmetric Synthesis of 2-Substituted Alcohols. -The key steps in the synthesis of the title alcohols are nucleophilic addition to the aldehyde (I), which p

(R)- and (S)-3-Hydroxy-4,4-dimethyl-1-ph

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ChemInform Abstract: (R)- and (S)-3-Hydr

ChemInform Abstract: (R)- and (S)-3-Hydroxy-4,4-dimethyl-1-phenyl-2-pyrrolidinone as Chiral Auxiliaries in the Enantioselective Preparation of α-Amino Acids.

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