(Q56952690)

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Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides

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scholarly article

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Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides (English)

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diastereoselectivity

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based on heuristic

inferred from title

Tom D. Sheppard

object named as

Tom D. Sheppard

7

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Félix Rodríguez

object named as

Félix Rodríguez

6

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object named as

Steven V. Ley

1

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author name string

Darren J. Dixon

2

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Richard T. Guy

3

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Maria A. Palomero

4

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Alessandra Polara

5

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publication date

2004

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Organic and Biomolecular Chemistry

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2

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24

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3618-3627

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Asymmetric hydroxylation of enolates with N-sulfonyloxaziridines

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Preparation of enantiopure butane-2,3-diacetals of glycolic acid and alkylation reactions leading to α-hydroxyacid and amide derivatives

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Highly Diastereoselective Lithium Enolate Aldol Reactions of Butane-2,3-diacetal Desymmetrized Glycolic Acid and Deprotection to Enantiopureanti-2,3-Dihydroxy Esters

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

1,2-Diacetals: A New Opportunity for Organic Synthesis

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Highly Diastereoselective Michael Addition Reactions of Butane-2,3-diacetal Desymmetrized Glycolic Acid. Preparation of α-Hydroxy-γ-amino Acid Derivatives

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Studies towards the total synthesis of rapamycin: Preparation of the C10C17 carbon unit

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Rapamycin (AY-22,989), a new antifungal antibiotic. I. Taxonomy of the producing streptomycete and isolation of the active principle

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Total Synthesis ofl-Biopterin froml-Tartaric Acidvia5-Deoxy-l-arabinose

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

An inexpensive carbohydrate derivative used as a chiral auxiliary in the synthesis of α-hydroxy carboxylic acids

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Utilisation d'alkoxyacetates chiraux - equivalents de l'hydroxyacetaldehyde - en aldolisation stereocontrolee approche enantio et diastereoselective de polyols vicinaux

1 reference

https://api.crossref.org/works/10.1039%2FB412790K

21 January 2018

Identifiers

10.1039/B412790K

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