Results 51 to 60 of about 4,668 (189)

An Efficient Synthesis of Acenaphtho[1,2-b]indole Derivatives via Domino Reaction

open access: yesMolecules, 2018
A concise and efficient synthesis of acenaphtho[1,2-b]indole derivatives via the domino reactions of enaminones with acenaphthoquinone catalyzed by l-proline has been developed. This protocol has the advantages of good yields, operational convenience and
Guo-Ning Zhang   +5 more
doaj   +1 more source

Transition-metal-free synthesis of 3-sulfenylated chromones via KIO3-catalyzed radical C(sp2)–H sulfenylation

open access: yesBeilstein Journal of Organic Chemistry, 2017
The reactions between o-hydroxylphenyl-functionalized enaminones and sulfonyl hydrazines providing 3-sulfenylated chromones via domino chromone ring construction and C(sp2)–H bond sulfenylation have been achieved under transition-metal-free conditions by
Yanhui Guo   +3 more
doaj   +1 more source

Sequentially Palladium-Catalyzed Processes in One-Pot Syntheses of Heterocycles

open access: yesApplied Sciences, 2015
Sequentially Pd-catalyzed processes are excellent entries to heterocycle synthesis. The broad mechanistic variety combined with often very mild reaction conditions allow the concatenation of elementary organic and organometallic steps to novel sequences ...
Timo Lessing, Thomas J. J. Müller
doaj   +1 more source

Recent Advances in Organocatalyzed Domino C–C Bond-Forming Reactions

open access: yesMolecules, 2017
Reactions that form a C–C bond make up a foundational pillar of synthetic organic chemistry. In addition, organocatalysis has emerged as an easy, environmentally-friendly way to promote this type of bond formation. Since around 2000, organocatalysts have
Cleo S. Evans, Lindsey O. Davis
doaj   +1 more source

Organocatalytically Generated Donor-Acceptor Cyclopropanes in Domino Reactions. One-Step Enantioselective Synthesis of Pyrrolo[1,2-a]quinolines.

open access: yesOrganic Letters, 2016
An easy and straightforward procedure has been developed for the synthesis of highly enantioenriched pyrrolo[1,2-a]quinolines through a one-pot process that comprises a domino cyclopropane ring opening/aza-Michael/aldol reaction followed by acid-promoted
Eduardo Sánchez-Díez   +5 more
semanticscholar   +1 more source

Synthesis of (–)-Indolizidine 167B based on domino hydroformylation/cyclization reactions

open access: yesBeilstein Journal of Organic Chemistry, 2008
The synthesis of (–)-Indolizidine 167B has been achieved from optically active (R)-3-(pyrrol-1-yl)hex-1-ene. The key step is a highly regioselective hydroformylation reaction and a one-pot intramolecular cyclization providing a general approach to the ...
Giuditta Guazzelli   +2 more
doaj   +1 more source

Crystal structure of racemic [(1R,2S,3R,4S,6S)-2,6-bis(furan-2-yl)-4-hydroxy-4-(thiophen-2-yl)cyclohexane-1,3-diyl]bis(thiophen-2-ylmethanone)

open access: yesActa Crystallographica Section E: Crystallographic Communications, 2016
In the title compound, C28H22O5S3, the central cyclohexane ring adopts a chair conformation. The atoms of the furan ring attached to the 6-position of the central cyclohexane ring are disordered over two sets of sites with occupancies of 0.832 (5) and 0 ...
Ísmail Çelik   +4 more
doaj   +1 more source

CuI-catalyzed domino reactions for the synthesis of benzoxazine-fused isoquinolines under microwave irradiation

open access: yes, 2016
A small library of benzoxazine-fused isoquinolines has been synthesized under microwave irradiation (MW) via CuI-catalyzed domino reactions of o-alkynyl aldehydes and amines having embedded nucleophiles.
Yunhui Zhao   +5 more
semanticscholar   +1 more source

Kinetics Studies on a Multicomponent Knoevenagel−Michael Domino Reaction by an Automated Flow Reactor

open access: yesChemistryOpen, 2019
The optimization of complex chemical reaction systems is often a troublesome and time‐consuming process. The application of modern technologies, including automated reactors and analytics, opens the avenue for generating large data sets on chemical ...
Christian P. Haas, Prof. Ulrich Tallarek
doaj   +1 more source

An efficient synthesis of the guaiane sesquiterpene (−)-isoguaiene by domino metathesis

open access: yesBeilstein Journal of Organic Chemistry, 2019
(−)-Isoguaiene was prepared from (S)-citronellal in only 9–10 steps with good overall yields. Either a trienyne or a dienediyne metathesis and highly diastereoselective organocatalytic Michael additions of aldehydes derived from (S)-citronellal served as
Yuzhou Wang   +3 more
doaj   +1 more source

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