Results 101 to 110 of about 25,619 (230)
Over the last several years there has been a huge increase in the development and applications of new efficient organocatalysts for enantioselective pericyclic reactions, which represent one of the most powerful types of organic transformations.
Felix E. Held +2 more
doaj +1 more source
The present study describes an efficient and ecofriendly, ultrasound, one-pot click cycloaddition approach for the construction of a novel series of 1,4-disubstituted-1,2,3-triazoles tethered with fluorinated 1,2,4-triazole-benzothiazole molecular ...
Rezki Nadjet, Aouad Mohamed Reda
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A facile synthesis of dispirooxindolopyrrolidines has been accomplished via a one-pot three component 1,3-dipolar cycloaddition reaction. The reaction of azomethine ylides generated in situ from L-phenylalanine and substituted isatins with a series of ...
Abdulrahman I. Almansour +5 more
doaj +1 more source
One-flask synthesis of 1,3,5-trisubstituted 1,2,4- triazoles from nitriles and hydrazonoyl chlorides via 1,3-dipolar cycloaddition [PDF]
[[abstract]]A new “one-flask” synthesis of 3,5-disubstituted 1,2,4-triazoles has successfully been developed to synthesize a series of 3,5-disubstituted 1,2,4-triazoles.
Wang, Li-Ya;Wang, Li-Ya;蔡建鈞;Tsai, Henry J;Lin, Hui-Yi;Lin, Hui-Yi;Ka, Kimiyoshi;Kaneko, Kimiyoshi;Che, Fen-Ying;Cheng, Fen-Ying;Sh, Hsin-Siao;Shih, Hsin-Siao;Won, Fung Fuh;Wong, Fung Fuh;Hu, Jiann-Jyh;Huang, Jiann-Jyh
core
This study focuses on synthesizing a new series of isoxazolinyl-1,2,3-triazolyl-[1,4]-benzoxazin-3-one derivatives 5a–5o. The synthesis method involves a double 1,3-dipolar cycloaddition reaction following a “click chemistry” approach, starting from the ...
Mohamed Ellouz +12 more
doaj +1 more source
A new series of 1,3,4,5,5-pentasubstituted-1,2,4-triazoles (4a–j, 6a–j) have been synthesized by the 1,3-dipolar cycloaddition of suitable nitrilimines 2 to pyruvaldehyde (2-oxopropanal) hydrazones having (COPh, COOMe, COOEt, Me/Me, and Me/Ph) groups 3 ...
Hany M. Dalloul
doaj +1 more source
Cycloaddition Reactions of C,N-Diphenylnitrone to Methylene-γ-butyrolactones
Cycloaddition of C,N-diphenylnitrone to α-methylene-γ-butyrolactone afforded two diastereomeric 5-spirosubstituted isoxazolidines with high selectivity.
Andrea Goti +3 more
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1, 3-Dipolar cycloaddition of aldehyde hydrazones with dimethyl acetylenedicarboxylate without solvent gives rise to dimethyl 1, 3-diphenylpyrazole-4, 5-dicarboxylate, and in some cases trimethyl 1-phenylpyrazole-3, 4, 5-tricarboxylate as a by-product.
OGURA, HARUO +3 more
openaire +2 more sources
Aspects of the chemistry of some highly crowded aromatic ligands [PDF]
A series of ortho-substituted arylchlorophosphoranes has been prepared. The structures of these compounds have been studied by the use of (^31)Cl n.q.r. and solid-state (^31)P n.m.r. . It has been shown that ortho substitution by groups such as CH(_3) or
Straw, T. A.
core
3-Functional substituted 4-trifluoromethyl tetrahydrothiophenes via [3 + 2]-cycloaddition reactions [PDF]
New 4-(trifluoromethyl)tetrahydrothiophenes containing an ester, sulfone, sulfoximine, sulfonamide, or phosphonate moiety at position 3 were synthesized by 1,3-dipolar [3 + 2]-cycloaddition reactions of 3,3,3-trifluoropropene derivatives and thiocarbonyl
Yuriy G. Shermolovich (2528338) +4 more
core +1 more source

