Catalytic Asymmetric Hetero-Diels-Alder Reactions of Carbonyl Compounds and Imines (Q34089234)

30 July 2017

title

Catalytic Asymmetric Hetero-Diels-Alder Reactions of Carbonyl Compounds and Imines (English)

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30 July 2017

Jørgensen KA

1

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30 July 2017

publication date

1 October 2000

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30 July 2017

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30 July 2017

volume

39

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30 July 2017

issue

20

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30 July 2017

page(s)

3558-3588

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Synthesen in der hydroaromatischen Reihe

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Catalytic asymmetric glyoxylate-ene reaction: a practical access to .alpha.-hydroxy esters in high enantiomeric purities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Asymmetric ene reactions in organic synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Asymmetric hetero Diels-Alder reactions and ene reactions catalyzed by chiral copper(II) complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Development of an unusually highly enantioselective hetero-Diels-Alder reaction of benzaldehyde with activated dienes catalyzed by hypercoordinating chiral aluminum complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

First application of attractive intramolecular interactions to the design of chiral catalysts for highly enantioselective Diels-Alder reactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

The origin of greater than 200:1 enantioselectivity in a catalytic Diels-Alder reaction as revealed by physical and chemical studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Demonstration of the Synthetic Power of Oxazaborolidine-Catalyzed Enantioselective Diels-Alder Reactions by Very Efficient Routes to Cassiol and Gibberellic Acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

A Highly Enantioselective Hetero-Diels-Alder Reaction Catalyzed by Chiral Polybinaphthyl-Aluminum Complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Chiral semicorrins and related nitrogen heterocycles as ligands in asymmetric catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Chiral bis(oxazoline) copper(II) complexes: versatile catalysts for enantioselective cycloaddition, Aldol, Michael, and carbonyl ene reactions

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

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Chemistry of spiroketals

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Acarbose. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Acarbose : An Update of its Pharmacology and Therapeutic Use in Diabetes Mellitus

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Rational design of potent sialidase-based inhibitors of influenza virus replication

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

New approaches to influenza chemotherapy. Neuraminidase inhibitors

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Recent developments in the stereoselective synthesis of α-aminoacids

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Selective reactions using allylic metals

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Catalytic Enantioselective Addition to Imines

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

New developments in the enantioselective synthesis of cyclopentyl carbocyclic nucleosides

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

An Efficient Asymmetric Approach to Carbocyclic Nucleosides: Asymmetric Synthesis of 1592U89, a Potent Inhibitor of HIV Reverse Transcriptase

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

21 January 2018

Carbocyclic nucleosides

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Catalytic enantioselective aza-Diels-alder reactions of imines--an approach to optically active nonproteinogenic alpha-amino acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Asymmetric Hetero Diels-Alder Reactions

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Conformations of Chiral α,β-Unsaturated Sulfoxides and Their Complexes with Lewis Acids. An ab Initio Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Bis(oxazoline) and Bis(oxazolinyl)pyridine Copper Complexes as Enantioselective Diels−Alder Catalysts: Reaction Scope and Synthetic Applications

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Chiral Bis(oxazoline)copper(II) Complexes as Lewis Acid Catalysts for the Enantioselective Diels−Alder Reaction

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Asymmetric tandem Mannich-Michael reactions of amino acid ester imines with Danishefsky's diene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Asymmetric synthesis of indolo[2,3-a]quinolizidin-2-ones - congeners to yohimbine-type alkaloids

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

Asymmetric synthesis of highly functionalized tetracyclic indole bases embodying the basic skeleton of yohimbine- and reserpine type alkaloids

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1 reference

https://api.crossref.org/works/10.1002%2F1521-3773%2820001016%2939%3A20%3C3558%3A%3AAID-ANIE3558%3E3.0.CO%3B2-I

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1 reference

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1 reference

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Reactions of ketene silyl acetals with imine-complexes of titanium tetrachloride. New and convenient routes to 5,6-dihydro-2-pyridones and 5-amino-2-alkenoates

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1 reference

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Bis(oxazolines) as chiral ligands in metal-catalyzed asymmetric reactions. Catalytic, asymmetric cyclopropanation of olefins

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1 reference

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1 reference

20 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1016/0040-4039(91)80110-R

Identifiers

DOI

10.1002/1521-3773(20001016)39:20<3558::AID-ANIE3558>3.0.CO;2-I

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30 July 2017

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