A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids (Q56853348)

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English	A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids	No description defined

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title

A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids (English)

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main subject

enantioselectivity

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inferred from title

chirality

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author

Elias James Corey

series ordinal

1

object named as

E.J Corey

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author name string

Raman K Bakshi

series ordinal

2

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publication date

January 1990

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published in

Tetrahedron Letters

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volume

31

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issue

5

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page(s)

611-614

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cites work

Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications

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Crossref

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https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2994581-7

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7 January 2021

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A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses

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https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2994581-7

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7 January 2021

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An efficient and catalytically enantioselective route to (S)-(-)-phenyloxirane

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7 January 2021

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Robert Robinson Lecture. Retrosynthetic thinking—essentials and examples

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https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2994581-7

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Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

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reference URL

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7 January 2021

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Identifiers

DOI

10.1016/S0040-4039(00)94581-7

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