Results 11 to 20 of about 11,460 (224)

Zinc-Catalyzed β-Allylation of Cyclopropanols via Enolized Homoenolate [PDF]

open access: yes, 2021
We report herein a zinc-catalyzed β-allylation of cyclopropanols with Morita–Baylis–Hillman (MBH) carbonates with retention of the cyclopropane ring.
Naohiko, Yoshikai, Yoshiya, Sekiguchi
core   +2 more sources

Catalytic Asymmetric Defluorinative Allylation of Silyl Enol Ethers [PDF]

open access: yes, 2023
The stereocontrolled installation of alkyl fragments at the alpha position of ketones is a fundamental yet unresolved transformation in organic chemistry.
Albert, Moyano   +3 more
core   +2 more sources

Organophotoredox/Ni-Cocatalyzed Allylation of Allenes: Regio-, and Diastereoselective Access to Homoallylic Alcohols [PDF]

open access: yes, 2021
A dual organophotoredox/nickel-catalyzed reductive coupling of allenes with aldehydes has been developed for the rapid assembly of anti-homoallylic alcohols with high levels of regioselectivities (>20:1), and diastereoselectivities (up to >20:1) and ...
Hui, Xie, Bernhard, Breit
core   +1 more source

Latent Pronucleophiles in Lewis Base Catalysis: Enantioselective Allylation of Silylated Stabilized Carbon Nucleophiles with Allylic Fluorides [PDF]

open access: yes, 2023
Lewis base catalyzed allylations of C-centered nucleophiles have been largely limited to the niche substrates with acidic C-H substituted with C-F bonds at the stabilized carbanionic carbon.
Markus, Lange   +4 more
core   +1 more source

Sustainability and efficiency assessment of lignin-derived phenolic synthons’ allylation: in solution versus ball-milling [PDF]

open access: yes, 2022
Allylation of phenols, a widely used reaction in multistep synthetic pathways, was herein investigated using mechanochemistry. This synthesis was first optimized on vanillin by varying key parameters including both chemical (e.g., stoichiometry, reaction
Sami, FADLALLAH   +5 more
core   +2 more sources

Enantioselective Allylation from Allene, a Petroleum Cracking Byproduct [PDF]

open access: yes, 2018
Allene (C3H4) gas is produced and separated on million-metric-ton scale per year during petroleum refining but is only rarely employed in chemical manufacturing. Meanwhile, the addition of an allyl group (C3H5) to ketone-containing molecules is among the
Yujing, Zhou   +3 more
core   +2 more sources

Rapid Decarboxylative Allylation of Nitroalkanes

open access: yes, 2016
Allyl nitroacetates undergo decarboxylative allylation to provide tertiary nitroalkanes in high yield. Moreover, the transformations are complete within several minutes under ambient conditions. High yields result because O-allylation of the intermediate
Alexander J. Grenning (2167951)   +1 more
core   +3 more sources

Highly Diastereo- and Enantioselective Allylboration of Aldehydes using alpha-Substituted Allyl/Crotyl Pinacol Boronic Esters via in Situ Generated Borinic Esters [PDF]

open access: yes, 2013
Readily available, alpha-substituted allyl/crotyl pinacol boronic esters often give low E/Z selectivity (with Z favored) in reactions with aldehydes. We found that addition of nBuLi to the pinacol boronic ester followed by trapping of the alkoxide with ...
Jack L.‐Y. Chen   +10 more
core   +1 more source

Highly Enantio‐ and Diastereoselective Synthesis of Tetrahydrofuran Frameworks via Chiral Lewis Acid‐Catalyzed Formal [3+2] Cycloaddition of Allylsilanes

open access: yesAngewandte Chemie, EarlyView.
The first catalytic asymmetric formal [3+2] cycloaddition of allylsilanes delivers cis‐2,5‐disubstituted tetrahydrofuran‐3‐ones that serve as versatile intermediates for the synthesis of diverse bioactive scaffolds. ABSTRACT A formal [3+2] cycloaddition via cyclization/1,2‐hydride shift initiated by nucleophilic attack of allylsilanes has been ...
Hosung Lee   +5 more
wiley   +2 more sources

Modular allylation of C(sp3)−H bonds by combining decatungstate photocatalysis and HWE olefination in flow [PDF]

open access: yes, 2021
The late-stage introduction of allyl groups provides an opportunity to synthetic organic chemists for subsequent diversification, providing rapid access to new chemical space.
Timothy, Noel   +4 more
core   +2 more sources

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