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New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction

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New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction (English)

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David W. C. MacMillan

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Kateri A. Ahrendt

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1

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Christopher J. Borths

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2

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language of work or name

English

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publication date

May 2000

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published in

Journal of the American Chemical Society

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volume

122

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issue

17

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page(s)

4243-4244

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cites work

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA000092S

Asymmetric synthesis of bicyclic intermediates of natural product chemistry

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA000092S

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA000092S

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA000092S

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA000092S

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10.1021/JA000092S

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(Q55968184)

New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction

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