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Record W2330636615 · doi:10.1021/om500520z

Palladium-Catalyzed Suzuki–Miyaura Cross-Couplings with 2-Diethylphosphonato-Substituted Aryl- and Naphthylboronate Esters as the Nucleophilic Partner: A Complementary Approach to the Synthesis of Biaryl Monophosphonates

2014· article· en· W2330636615 on OpenAlexaff
Simon Doherty, Julian G. Knight, Nicholas A. Ward, Daniel O. Perry, Dror M. Bittner, Michael R. Probert, Stephen A. Westcott

Bibliographic record

VenueOrganometallics · 2014
Typearticle
Languageen
FieldChemistry
TopicCatalytic Cross-Coupling Reactions
Canadian institutionsMount Allison University
FundersEngineering and Physical Sciences Research CouncilNewcastle University
KeywordsChemistryPhosphonateNucleophileArylYield (engineering)Steric effectsPalladiumElectrophileCombinatorial chemistryCatalysisOrganic chemistryPhosphineNucleophilic aromatic substitutionCoupling reactionMedicinal chemistryStereochemistryNucleophilic substitutionAlkyl

Abstract

fetched live from OpenAlex

This paper reports the first examples of Suzuki–Miyaura cross-couplings involving aryl- and naphthylphosphonate-based boronate esters as the nucleophilic partner. A systematic comparison of the performance of biaryl-like KITPHOS- and XPHOS-based systems revealed that, between them, an electronically and sterically diverse range of substrates can be coupled with remarkable efficiency to afford high yields of the corresponding biaryl and heterobiaryl monophosphonates. The use of an aryl- and naphthylphosphonate-based boronate ester as the coupling partner presents an alternative and potentially complementary pathway to existing couplings in which the aryl- or naphthylphosphonate unit is typically introduced as the electrophile. The potential advantages associated with the use of this new class of coupling partner were clearly demonstrated by the palladium-catalyzed reaction between diethyl [2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]phosphonate and 1-bromo-2-methoxynaphthalene that gave the corresponding biaryl monophosphonate in 56% yield, a marked improvement on the 6% yield obtained from the reaction between 2-methoxy-1-naphthylboronic acid and diethyl (2-bromophenyl)phosphonate with the same catalyst under the same conditions. The potential utility of this new coupling combination was demonstrated by reducing one of the products, 2-methoxy-1-(2′-diethoxyphosphorylphenyl)naphthylene, to the corresponding primary phosphine, which was subsequently converted into a diastereoisomeric mixture of the R, R -hexane-2,5-diol-derived phospholane in reasonable yield.

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.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation 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 score0.002
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.002

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 head0.011
GPT teacher head0.239
Teacher spread0.228 · 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

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations13
Published2014
Admission routes1
Has abstractyes

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