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Record W1966513519 · doi:10.1021/ja908316n

[Ir(COD)Cl]<sub>2</sub> as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation

2009· article· en· W1966513519 on OpenAlex
Kevin D. Hesp, Sven Tobisch, Mark Stradiotto

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenueJournal of the American Chemical Society · 2009
Typearticle
Languageen
FieldChemistry
TopicAsymmetric Hydrogenation and Catalysis
Canadian institutionsDalhousie University
Fundersnot available
KeywordsHydroaminationChemistryCatalysisIntramolecular forceMedicinal chemistryAminationAlkylKinetic isotope effectPhosphineArrhenius equationOrganic chemistryActivation energy

Abstract

fetched live from OpenAlex

The successful application of [Ir(COD)Cl](2) as a precatalyst for the intramolecular addition of primary as well as secondary alkyl- or arylamines to unactivated olefins at relatively low catalyst loading is reported (25 examples), along with a comprehensive experimental and computational investigation of the reaction mechanism. Catalyst optimization studies examining the cyclization of N-benzyl-2,2-diphenylpent-4-en-1-amine (1a) to the corresponding pyrrolidine (2a) revealed that for reactions conducted at 110 degrees C neither the addition of salts (N(n)Bu(4)Cl, LiOTf, AgBF(4), or LiB(C(6)F(5))(4) x 2.5 OEt(2)) nor phosphine coligands served to enhance the catalytic performance of [Ir(COD)Cl](2). In this regard, the rate of intramolecular hydroamination of 1a employing [Ir(COD)Cl](2)/L2 (L2 = 2-(di-t-butylphosphino)biphenyl) catalyst mixtures exhibited an inverse-order dependence on L2 at 65 degrees C, and a zero-order rate dependence on L2 at 110 degrees C. However, the use of 5 mol % HNEt(3)Cl as a cocatalyst was required to promote the cyclization of primary aminoalkene substrates. Kinetic analysis of the hydroamination of 1a revealed that the reaction rate displays first order dependence on the concentration of Ir and inverse order dependence with respect to both substrate (1a) and product (2a) concentrations; a primary kinetic isotope effect (k(H)/k(D) = 3.4(3)) was also observed. Eyring and Arrhenius analyses for the cyclization of 1a to 2a afforded DeltaH(double dagger) = 20.9(3) kcal mol(-1), DeltaS(double dagger) = -23.1(8) cal/K x mol, and E(a) = 21.6(3) kcal mol(-1), while a Hammett study of related arylaminoalkene substrates revealed that increased electron density at nitrogen encourages hydroamination (rho = -2.4). Plausible mechanisms involving either activation of the olefin or the amine functionality have been scrutinized computationally. An energetically demanding oxidative addition of the amine N-H bond to the Ir(I) center precludes the latter mechanism and instead activation of the olefin C=C bond prevails, with [Ir(COD)Cl(substrate)] M1 representing the catalytically competent compound. Notably, such an olefin activation mechanism had not previously been documented for Ir-catalyzed alkene hydroamination. The operative mechanistic scenario involves: (1) smooth and reversible nucleophilic attack of the amine unit on the metal-coordinated C=C double bond to afford a zwitterionic intermediate; (2) Ir-C bond protonolysis via stepwise proton transfer from the ammonium unit to the metal and ensuing reductive elimination; and (3) final irreversible regeneration of M1 through associative cycloamine expulsion by new substrate. DFT unveils that reductive elimination involving a highly reactive and thus difficult to observe Ir(III)-hydrido intermediate, and passing through a highly organized transition state structure, is turnover limiting. The assessed effective barrier for cyclohydroamination of a prototypical secondary alkylamine agrees well with empirically determined Eyring parameters.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.014
Threshold uncertainty score0.457

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0000.001
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.006
GPT teacher head0.214
Teacher spread0.209 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it