Photo-oxidative Cross-Dehydrogenative Coupling-Type Reaction of Thiophenes with α-Position of Carbonyls Using a Catalytic Amount of Molecular Iodine.
Sign Up to like & getrecommendations! Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b00428
Abstract: A metal-free photo-oxidative intermolecular C-H/C-H coupling reaction of thiophenes is demonstrated with carbonyls using a catalytic amount of molecular iodine. In this system, molecular oxygen in the air acted as a terminal oxidant to regenerate… read more here.
Keywords: carbonyls using; using catalytic; iodine; reaction thiophenes ... See more keywords
Dealkenylative Alkynylation Using Catalytic FeII and Vitamin C.
Sign Up to like & getrecommendations! Published in 2022 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.2c05980
Abstract: In this paper, we report the synthesis of alkyl-tethered alkynes through ozone-mediated and FeII-catalyzed dealkenylative alkynylation of unactivated alkenes in the presence of alkynyl sulfones. This one-pot reaction, which employs a combination of a catalytic… read more here.
Keywords: alkynylation; dealkenylative alkynylation; catalytic feii; using catalytic ... See more keywords
Synthesis of zeolite SSZ-24 using a catalytic amount of SSZ-13 seeds
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DOI: 10.1039/c9qi00971j
Abstract: The crystallisation of SSZ-24 is accelerated by using a catalytic amount of SSZ-13 (CHA) seeds. read more here.
Keywords: amount ssz; synthesis zeolite; using catalytic; ssz ... See more keywords
Synthesis of Tri- and Disubstituted Fluorenols and Derivatives Thereof Using Catalytic [2+2+2] Cyclotrimerization
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DOI: 10.3390/catal9110942
Abstract: A method for regioselective synthesis of 2,4-disubstituted and more highly substituted fluorenols using catalytic [2+2+2]cyclotrimerization of mono- and disubstituted diynes with terminal alkynes was explored. In the former case, the preferential formation of the 2,4-regioisomers… read more here.
Keywords: catalytic cyclotrimerization; tri disubstituted; synthesis tri; using catalytic ... See more keywords