A highly enantioselective intramolecular Heck reaction with a monodentate ligand (Q43848387)

27 November 2017

title

A highly enantioselective intramolecular Heck reaction with a monodentate ligand (English)

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27 November 2017

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Ben L Feringa

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Adriaan Jacobus Minnaard

series ordinal

object named as

Adriaan J Minnaard

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27 November 2017

Rosalinde Imbos

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27 November 2017

language of work or name

English

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publication date

1 January 2002

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Journal of the American Chemical Society

27 November 2017

published in

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27 November 2017

volume

124

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27 November 2017

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27 November 2017

page(s)

184-185

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Chiral monophosphines as ligands for asymmetric organometallic catalysis

27 November 2017

cites work

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

Highly Enantioselective or Not?-Chiral Monodentate Monophosphorus Ligands in the Asymmetric Hydrogenation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

Catalytic asymmetric carbon-carbon bond formation: asymmetric synthesis of cis-decalin derivatives by palladium-catalyzed cyclization of prochiral alkenyl iodides

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

Highly Enantioselective Rhodium-Catalyzed Hydrogenation with Monodentate Ligands

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

A catalytic asymmetric synthesis of hydrindans

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

Structure and bonding in a phosphenium ion-metal complex, CH3NCH2CH2N(CH3)PMo(.eta.5-C5H5)(CO)2. An example of a molybdenum-phosphorus multiple bond

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA017200A

Thwarting beta-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction This research was supported by the National Institutes of Health (grant GM-12389). M.O. thanks the Deutsche Forschungsgemein

1 reference

15 December 2024

https://opencitations.net/index/api/v1/references/10.1021/JA017200A

Improved catalysts for the palladium-catalyzed synthesis of oxindoles by amide alpha-arylation. Rate acceleration, use of aryl chloride substrates, and a new carbene ligand for asymmetric transformations

1 reference

15 December 2024

https://opencitations.net/index/api/v1/references/10.1021/JA017200A

Identifiers

DOI

10.1021/JA017200A

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27 November 2017

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