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Transition Metal Complexation in 1,3-Dipolar Cycloadditions

HETEROCYCLES, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
BROGGINI, GIANLUIGI   +3 more
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Dipolar Cycloaddition Reactions of Nitrilimines

Australian Journal of Chemistry, 1998
A series of ?-substituted a-methylidene-?-butyrolactone derivatives underwent regiospecific 1,3-dipolar cycloaddition with N -methyl- C -phenylnitrilimine. These reactions proceeded regiospecifically and with high diastereoselectivity, generally favouring the anti diastereomer as determined by n.m.r.
Dunstan, J.   +5 more
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Dipolar Cycloadditions of Nitrones in Aqueous Media

HETEROCYCLES, 2016
1,3-Dipolar cycloadditions of nitrones in aqueous media have been recently exploited as a non-conventional protocol in the synthesis of the fully- or partly-saturated isoxazole ring. Water as the reaction medium can affect positively both cycloaddition rates and yields, while the large array of latent functionalities displayed by the cycloadducts is of
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Concertedness of 1,3-dipolar cycloadditions

Journal of Chemical Education, 1984
The 1,3-dipolar cycloaddition is the union of a 1,3-dipole with a multiple bond system (a dipolarophile) to form a five-membered ring; the process is regarded as one of the most general methods for the synthesis of five-membered heterocycles.
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Dipolar Cycloadditions

2006
M. C. Carreño, M. Ribagorda
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Dipolar Cycloadditions

2012
A. Chanda, V. V. Fokin
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1,3-Dipolar Cycloaddition

2002
G. Hajos, Z. Riedl
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Asymmetric 1,3-Dipolar Cycloaddition Reactions

Chemical Reviews, 1998
Kurt V., Gothelf, Karl Anker, Jørgensen
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