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Journal ArticleDOI

Rhodium‐Catalyzed Dynamic Kinetic Asymmetric Transformations of Racemic Allenes by the [3+2] Annulation of Aryl Ketimines

Duc N. Tran, +1 more
- 27 Sep 2013 - 
- Vol. 52, Iss: 40, pp 10630-10634
TLDR
Racemization required: Rhodium(I)-catalyzed C-H activation directed by unprotected ketimines initiates selective [3+2] cycloaddition with allenes, providing access to highly substituted indenylamines.
Abstract
Keywords: allenes ; asymmetric catalysis ; CH activation ; DYKAT ; rhodium Reference EPFL-ARTICLE-190184doi:10.1002/anie.201304919View record in Web of Science Record created on 2013-11-04, modified on 2017-05-12

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Citations
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Journal ArticleDOI

Transition metal-catalyzed C–H bond functionalizations by the use of diverse directing groups

TL;DR: In this article, a review of the development of utilizing functionalities as directing groups for the construction of C-C and C-hetero bonds via C-H activation using various transition metal catalysts is presented.
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Catalytic Enantioselective Transformations Involving C-H Bond Cleavage by Transition-Metal Complexes.

TL;DR: This analysis comprehensively review all asymmetric transition-metal-catalyzed methodologies that are believed to proceed via an inner-sphere-type mechanism, with an emphasis on the nature of stereochemistry generation.
Journal ArticleDOI

Recent development of direct asymmetric functionalization of inert C–H bonds

TL;DR: The area of direct asymmetric functionalization of inert C-H bonds has attracted considerable attention in recent years as discussed by the authors, and a lot of strategies have emerged including asymmetric C−H bond insertion by metal carbenoids or analogs, cross dehydrogenative coupling, [1,5]-hydride transfer, C-h bond functionalization involving a transient metal-carbon species and other miscellaneous methods.
Journal ArticleDOI

Metal-Catalyzed Annulations through Activation and Cleavage of C-H Bonds.

TL;DR: The exponential increase in the number of catalytic transformations that involve a metal-promoted activation of hitherto considered inert C-H bonds is promoting a fundamental change in the field of synthetic chemistry.
Journal ArticleDOI

Advances in Stereoconvergent Catalysis from 2005 to 2015: Transition-Metal-Mediated Stereoablative Reactions, Dynamic Kinetic Resolutions, and Dynamic Kinetic Asymmetric Transformations

TL;DR: This Review summarizes major advances in nonenzymatic, transition-metal-promoted dynamic asymmetric transformations reported between 2005 and 2015.
References
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Journal ArticleDOI

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

TL;DR: This is the first comprehensive review encompassing the large body of work in this field over the past 5 years, and will focus specifically on ligand-directed C–H functionalization reactions catalyzed by palladium.
Journal ArticleDOI

Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.

TL;DR: A review of palladium-catalyzed coupling of CH bonds with organometallic reagents through a PdII/Pd0 catalytic cycle can be found in this paper.
Journal ArticleDOI

Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond Activation

TL;DR: This review focuses on Rh-catalyzed methods for C-H bond functionalization, which have seen widespread success over the course of the last decade and are discussed in detail in the accompanying articles in this special issue of Chemical Reviews.
Journal ArticleDOI

Aryl-aryl bond formation by transition-metal-catalyzed direct arylation.

TL;DR: A number of improvements have developed the former process into an industrially very useful and attractive method for the construction of aryl -aryl bonds, but the need still exists for more efficient routes whereby the same outcome is accomplished, but with reduced waste and in fewer steps.
Journal ArticleDOI

C–C, C–O and C–N bond formation via rhodium(III)-catalyzed oxidative C–H activation

TL;DR: The facile construction of C-E (E = C, N, S, or O) bonds makes Rh(III) catalysis an attractive step-economic approach to value-added molecules from readily available starting materials.
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