(Q64951641)

1 July 2019

title

ESTER DERIVED TITANIUM ENOLATE ALDOL REACTION: HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF SYN- AND ANTI-ALDOLS. (English)

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1 July 2019

author name string

Arun K Ghosh

1

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1 July 2019

Steve Fidanze

2

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1 July 2019

Masanobu Onishi

3

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1 July 2019

Khaja Azhar Hussain

4

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1 July 2019

publication date

1 October 1997

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1 July 2019

published in

Tetrahedron Letters

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1 July 2019

volume

38

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1 July 2019

issue

41

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page(s)

7171-7174

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1 July 2019

Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis

cites work

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7 January 2021

Highly Enantioselective Aldol Reaction: Development of a New Chiral Auxiliary from cis-1-Amino-2-hydroxyindan

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7 January 2021

Concerning the Boron-Mediated Aldol Reaction of Carboxylic Esters

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7 January 2021

Enantioselective synthesis of anti-.alpha.-methyl-.beta.-hydroxy esters through titanium tetrachloride-mediated aldol condensation

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7 January 2021

Computer-Assisted Design of Chiral Boron Enolates: A Novel, Highly Enantioselective Aldol Reaction for Thioacetates and Thiopropionates

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7 January 2021

Synthesis of Enantiomerically Pure Anti-Aldols: A Highly Stereoselective Ester-Derived Titanium Enolate Aldol Reaction

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7 January 2021

The Stereochemistry of the Ivanov and Reformatsky Reactions. I

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Stereoselective aldol reactions using ticl4 as stereochemical template

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7 January 2021

Chelation-controlled enantioselective synthesis of key intermediates for the preparation of carbapenem antibiotics PS-5 and 1.beta.-methyl-PS-5

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7 January 2021

Asymmetric alkylations and aldol reactions: (1S,2R)-2-aminocyclopentan-1-ol derived new chiral auxiliary

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7 January 2021

10.1016/S0040-4039(97)01765-6

Identifiers

DOI

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1 July 2019

PMC publication ID

6217984

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1 July 2019

PubMed publication ID

30407471

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1 July 2019