Results 51 to 60 of about 2,089,289 (186)

Highly Regioselective Construction of Spirocycles via Phosphine-Catalyzed [3 + 2]-Cycloaddition

open access: yes, 2016
A direct entry to spirocycles with low to moderate regioselectivity was achieved by triphenylphosphine-catalyzed [3 + 2]-cycloaddition of active exo-methylenecycles (1) and ethyl 2,3-butadienoate (2).
Xiyan Lu (1470865)   +2 more
core   +1 more source

Roles of Lewis Acid Catalysts in Diels‐Alder Reactions between Cyclopentadiene and Methyl Acrylate

open access: yesChemistryOpen, 2020
The Diels‐Alder reaction of cyclopentadiene with methyl acrylate catalyzed by AlCl3 has been theoretically investigated. M06‐2X level DFT calculations have shown that the formation of two C−C bonds is asynchronous in the cycloaddition both in the endo ...
Prof. Ken Sakata   +1 more
doaj   +1 more source

[6 + 2] AND [4 + 2] CYCLOADDITION REACTION OF DIPHENYLKETENE AND CYCLOHEPTATRIENE [PDF]

open access: yesJournal of Sciences, Islamic Republic of Iran, 1993
The cycloaddition reaction of diphenylketene and cycloheptatriene is studied. The reaction proceeds via a highly asynchronous reaction path to the zwitterionic 6 as intermediate. Subsequent CC- bond formation yields 8, 8 diphenylbicyclo [4. 2. I] nona-2,
doaj  

Ultrasound-promoted synthesis of novel fused heterocycles by criss-cross cycloaddition

open access: yesJournal of Saudi Chemical Society, 2016
This work reports a novel and highly efficient methodology for the synthesis of perhydrotriazolotriazoledithions from two successive 1,3-dipolar cycloaddition under ultrasound irradiation.
Javad Safari   +2 more
doaj   +1 more source

Synthesis of functionalised sulfonamides [PDF]

open access: yes, 2008
Sulfonamides are important therapeutic agents and have a diverse array of biological functions in biology and medicine. Their means of synthesis has often involved the use of unstable sulfonyl chloride species; however, recent research has established ...
Mok, B.L.
core  

A thermally-induced, tandem [3,3]-sigmatropic rearrangement/[2 + 2] cycloaddition approach to carbocyclic spirooxindoles

open access: yesBeilstein Journal of Organic Chemistry, 2010
The synthesis of C3-carbocyclic spirooxindoles was realized by way of an intramolecular [2 + 2] cycloaddition reaction between a vinylidene indolin-2-one and an alkyne.
Kay M. Brummond, Joshua M. Osbourn
doaj   +1 more source

Recent advances in the iron-catalyzed cycloaddition reactions

open access: yes, 2012
The rapid generation of molecular in a relatively easy manner has made the cycloaddition reaction a powerful tool in the synthesis of different membered ring compounds.
Wang ChunXiang, Wan BoShun, 万伯顺
core   +1 more source

Asymmetric isothiourea-catalysed formal [3+2] cycloadditions of ammonium enolates with oxaziridines [PDF]

open access: yes, 2015
The authors thank the Royal Society for a University Research Fellowship (A.D.S.) and the European Research Council under the European Union’s Seventh Framework Programme (FP7/2007—2013), ERC Grant Agreement No. 279850 (C.F.
McLennan, Ross   +14 more
core   +1 more source

Time-Resolved Mechanism of the Cycloaddition Reaction between Difluorocarbene and Norbornadiene [PDF]

open access: yes
Cycloaddition between difluorocarbene and norbornadiene is a stepwise process where a non-linear cheletropic transition state (TS1) leads to a diradical intermediate, followed by 1,2- and 1,4-addition.
Yuchen, Zhang   +2 more
core   +1 more source

An ab initio study of the mechanism of the cycloaddition reaction forming bicyclic compounds between vinylidene (H2C=C:) and ethylene [PDF]

open access: yesJournal of the Serbian Chemical Society, 2011
The mechanism of the cycloaddition reaction forming a bicyclic compounds between singlet vinylidene (H2C=C:) and ethylene was investigated using the CCSD(T)//MP2/6-31G* method. From the potential energy profile, it can be predicted that this reaction has
YONGQING LI, ZHENXIA LIAN, XIUHUI LU
doaj  

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