Alcohol Synthesis by Cobalt-Catalyzed Visible-Light-Driven Reductive Hydroformylation

Nontraditional Fragment Couplings of Alcohols and Carboxylic Acids: C(sp3)–C(sp3) Cross-Coupling via Radical Sorting

(2022) Holt A. Sakai et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Deoxytrifluoromethylation of Alcohols

(2022) Nicholas E. Intermaggio et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Insertion of Carbon Monoxide into the Terminal Co–O Bond in a Methoxocobalt(III) Complex via a Tuneable Mechanism

(2022) Jia Zhang et al.   ORGANOMETALLICS

Hydroformylation catalyzed by unmodified cobalt carbonyl under mild conditions

(2022) Baoxin Zhang et al.   SCIENCE

Visible-Light-Enhanced Cobalt-Catalyzed Hydrogenation: Switchable Catalysis Enabled by Divergence between Thermal and Photochemical Pathways

(2021) Lauren N. Mendelsohn et al.   ACS Catalysis

Using Light to Modify the Selectivity of Transition Metal Catalysed Transformations

(2021) Danijela Lunic et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Metallaphotoredox-enabled deoxygenative arylation of alcohols

(2021) Zhe Dong et al.   NATURE

Controlling Chemoselectivity of Catalytic Hydroboration with Light

(2021) Enrico Bergamaschi et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

In-Situ Bromination Enables Formal Cross-Electrophile Coupling of Alcohols with Aryl and Alkenyl Halides

(2021) Benjamin K. Chi et al.   ACS Catalysis

Visible‐light controlled divergent catalysis using a bench‐stable cobalt(I) hydride complex

(2020) Enrico Bergamaschi et al.   CHEMISTRY-A EUROPEAN JOURNAL

Highly active cationic cobalt(II) hydroformylation catalysts

(2020) Drew M. Hood et al.   SCIENCE

Synthesis and Reactivity of Organometallic Intermediates Relevant to Cobalt‐Catalyzed Hydroformylation

(2020) Connor S. MacNeil et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Redox-neutral organocatalytic Mitsunobu reactions

(2019) Rhydian H. Beddoe et al.   SCIENCE

Dual Rh−Ru Catalysts for Reductive Hydroformylation of Olefins to Alcohols

(2018) Fábio M. S. Rodrigues et al.   ChemSusChem

Exploring the Alcohol Stability of Bis(phosphine) Cobalt Dialkyl Precatalysts in Asymmetric Alkene Hydrogenation

(2018) Hongyu Zhong et al.   ORGANOMETALLICS

Highly Regio- and Enantioselective Copper-Catalyzed Reductive Hydroxymethylation of Styrenes and 1,3-Dienes with CO2

(2017) Yong-Yuan Gui et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Alcohols as alkylating agents in heteroarene C–H functionalization

(2015) Jian Jin et al.   NATURE

From Olefins to Alcohols: Efficient and Regioselective Ruthenium-Catalyzed Domino Hydroformylation/Reduction Sequence

(2013) Ivana Fleischer et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Hydroformylation in the Realm of Scents

(2013) Elena V. Gusevskaya et al.   ChemCatChem

Ruthenium-Catalyzed Hydroformylation/Reduction of Olefins to Alcohols: Extending the Scope to Internal Alkenes

(2013) Lipeng Wu et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Stereoinversion of tertiary alcohols to tertiary-alkyl isonitriles and amines

(2013) Sergey V. Pronin et al.   NATURE

Applied Hydroformylation

(2012) Robert Franke et al.   CHEMICAL REVIEWS

Tandem Hydroformylation/Hydrogenation of Alkenes to Normal Alcohols Using Rh/Ru Dual Catalyst or Ru Single Component Catalyst

(2012) Kohei Takahashi et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Primary Alcohols from Terminal Olefins: Formal Anti-Markovnikov Hydration via Triple Relay Catalysis

(2011) G. Dong et al.   SCIENCE

High-Yielding Tandem Hydroformylation/Hydrogenation of a Terminal Olefin to Produce a Linear Alcohol Using a Rh/Ru Dual Catalyst System

(2010) Kohei Takahashi et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Percent buried volume for phosphine and N-heterocyclic carbene ligands: steric properties in organometallic chemistry

(2010) Hervé Clavier et al.   CHEMICAL COMMUNICATIONS

Origin of Pressure Effects on Regioselectivity and Enantioselectivity in the Rhodium-Catalyzed Hydroformylation of Styrene with (S,S,S)-BisDiazaphos

(2010) Avery L. Watkins et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY