Allylboration of Ketones Catalyzed by BINOL Derivatives: Which Species Are Involved Depending on Substrate Reactivity?-Reference-Cited by-同舟云学术

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Allylboration of Ketones Catalyzed by BINOL Derivatives: Which Species Are Involved Depending on Substrate Reactivity?

Published:2024-09-11 Issue: Volume: Page:
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Martel Arnaud¹^ORCID,Zaier Rania¹,Braire Julien²^ORCID,Macé Aurélie²,Vidal Joelle²^ORCID,Lalli Claudia²^ORCID,Carreaux François²^ORCID

Affiliation:

1. Institut des Molécules et Matériaux du Mans, IMMM UMR 6283 CNRS−Le Mans Université, Avenue Olivier Messiaen, 72085 Le Mans CEDEX 9, France.

2. Université de Rennes, CNRS, ISCR (Institut des Sciences Chimiques de Rennes) UMR 6226, 263 Avenue du Général Leclerc, Campus de Beaulieu, F-35000 Rennes, France.

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c01343

Reference30 articles.

1. Recent Advances in the Preparation and Application of Allylboron Species in Organic Synthesis

2. The Mechanism and an Improved Asymmetric Allylboration of Ketones Catalyzed by Chiral Biphenols

3. Mechanistic Insights into the Catalytic Asymmetric Allylboration of Ketones: Brønsted or Lewis Acid Activation?

4. BINOL derivatives-catalysed enantioselective allylboration of isatins: application to the synthesis of (R)-chimonamidine

5. Catalytic Enantioselective Allylboration and Related Reactions of Isatins Promoted by Chiral BINOLs: Scope and Mechanistic Studies

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