Results 11 to 20 of about 71,058 (285)

Mechanism, reactivity, and selectivity of nickel-catalyzed [4 + 4 + 2] cycloadditions of dienes and alkynes. [PDF]

open access: yes, 2014
Density functional theory (DFT) calculations with B3LYP and M06 functionals elucidated the reactivities of alkynes and Z/E selectivity of cyclodecatriene products in the Ni-catalyzed [4 + 4 + 2] cycloadditions of dienes and alkynes.
Baran, Phil S   +4 more
core   +5 more sources

Generation of Sulfonylated Tetrazoles through an Iron-Catalyzed Multicomponent Reaction Involving Sulfur Dioxide

open access: yesiScience, 2020
Summary: As a privileged motif, tetrazoles can be widely found in pharmaceuticals and materials science. Herein, a five-component reaction of cycloketone oxime esters, alkynes, DABCO·(SO2)2, and two molecules of trimethylsilyl azide under iron catalysis ...
Jun Zhang   +3 more
doaj   +1 more source

A frustrated-Lewis-pair approach to catalytic reduction of alkynes to cis-alkenes [PDF]

open access: yes, 2013
Frustrated Lewis pairs are compounds containing both Lewis acidic and Lewis basic moieties, where the formation of an adduct is prevented by steric hindrance.
Chernichenko, K.   +2 more
core   +1 more source

Nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts enabled by NN2 pincer ligand

open access: yesNature Communications, 2021
Alkynes are amongst the most valuable functional groups in organic chemistry, however, the preparation of alkyl-substituted alkynes still remains elusive. Here the authors show a nickel-catalyzed deaminative Sonogashira coupling of alkylpyridinium salts.
Xingjie Zhang   +4 more
doaj   +1 more source

Alkynes as Synthetic Equivalents of Ketones and Aldehydes: A Hidden Entry into Carbonyl Chemistry

open access: yesMolecules, 2019
The high energy packed in alkyne functional group makes alkyne reactions highly thermodynamically favorable and generally irreversible. Furthermore, the presence of two orthogonal π-bonds that can be manipulated separately enables flexible synthetic ...
Igor V. Alabugin   +4 more
doaj   +1 more source

[3+2] Cycloaddition of alkyl aldehydes and alkynes enabled by photoinduced hydrogen atom transfer

open access: yesNature Communications, 2022
In contrast to the prevalence of 1,3-dipolar cycloadditions, radical [3+2] annulations of alkynes are underexplored. Here, the authors describe [3+2] cycloadditions of various internal alkynes with readily accessible aliphatic aldehydes via photoinduced ...
Siya Le   +6 more
doaj   +1 more source

Synthesis of aryl-1H-1,2,3-triazoles via 1,3-dipolar cycloaddition

open access: yesOrbital: The Electronic Journal of Chemistry, 2012
A series of Aryl-1H-1,2,3-triazoles were prepared from the reaction between aril-azide (1) with 1.5 equiv. of terminal alkynes (2a-o). The reactions carried out at room temperature and in the presence of CuI (10 mol%) in acetonitrile. The compounds (3a-o)
Wagner O. Valença   +2 more
doaj   +1 more source

Isoprene oxidation by the gram-negative model bacterium variovorax sp. WS11 [PDF]

open access: yes, 2020
Plant-produced isoprene (2-methyl-1,3-butadiene) represents a significant portion of global volatile organic compound production, equaled only by methane.
Crombie, Andrew T.   +4 more
core   +1 more source

Reactions of Tetracyclone Molybdenum Complexes with Electrophilic Alkynes: Cyclopentadienone–Alkyne Coupling and Alkyne Coordination [PDF]

open access: yesOrganometallics, 2017
The reactions of the complexes [Mo(CO)2(η4-C4Ph4CO)2] and [Mo(CO)3(NCMe)(η4-C4Ph4CO)] with the alkynes dimethyl acetylenedicarboxylate (DMAD; RC≡CR where R = CO2Me) and methyl propiolate (RC≡CH) have been studied. In the case of DMAD, the initial product is the green carbonyl complex [Mo(CO)(RC≡CR)(η5,σ-C4Ph4COCR═CR)] (3), in which two alkyne molecules
Adams, H.   +4 more
openaire   +2 more sources

Iodine-mediated hydration of alkynes on keto-functionalized scaffolds: mechanistic insight and the regiospecific hydration of internal alkynes

open access: yesBeilstein Journal of Organic Chemistry, 2019
An iodine-mediated hydration reaction of alkynes serves as a green alternative to metal-catalyzed procedures. Previous work has shown that this method works well with terminal alkynes on keto-functionalized scaffolds, including 1,3-dicarbonyls and their ...
Zachary Lee   +8 more
doaj   +1 more source

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