Results 161 to 170 of about 8,699 (217)

Influence of the Nature of Group 15 Element on [Au^I]-C≡E/Azide 1,3-Dipolar Cycloaddition Reaction. [PDF]

Inorg Chem
González-Pinardo D, Fernández I.
europepmc   +1 more source

Solvent Effects on the Selectivity of Ambimodal Dipolar/Diels-Alder Cycloadditions: A Study Using Explicit Solvation Models. [PDF]

Chemphyschem
Matsubuchi H, Hayashi D, Okamoto D, Noguchi A, Nakagawa S, Takayanagi T, Murakami T.   +6 more
europepmc   +1 more source

A Remarkable Selectivity Observed in Hetero-Diels-Alder Reactions of Levoglucosenone (LGO) with Thiochalcones: An Experimental and Computational Study. [PDF]

Molecules
Mlostoń G, Urbaniak K, Palusiak M, Würthwein EU, Reissig HU, Witczak ZJ.   +5 more
europepmc   +1 more source

Dimerisation of aryl-substituted bicyclobutanes (BCBs): revealing a new mode of 1,3-dipolar background reactivity. [PDF]

Chem Sci
George M, Knyazev DA, Swiatek K, von Köller HF, Werz DB.   +4 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions

Chemical Reviews, 2008
Levi M, Stanley, Mukund P, Sibi
openaire   +4 more sources

Natural 1,3‐Dipolar Cycloadditions

Angewandte Chemie International Edition, 2015
[3+2] in the wild: Biomimetic natural product syntheses and theoretical considerations have indicated that 1,3-dipolar cycloadditions take place in nature. Now, the structure, biosynthesis, and function of a heavily modified prenylated flavin cofactor have been elucidated.
Martin, Baunach, Christian, Hertweck
openaire   +2 more sources

Extended dipolar cycloadditions

Journal of the Chemical Society, Perkin Transactions 1, 1975
Whilst the simple azomethine imine (5) undergoes the expected 1,3-dipolar cycloaddition to acetylenic esters, the extended azomethine imines (1) undergo 1,5-rather than 1,3-dipolar cycloaddition to give benzo[c][1,2,5]-triazepino[1,2-a]cinnolines (2), possibly by a stepwise mechanism 2-Alkyl-2λ5σ3-naphtho[1,8-de]triazines (12) and 2λ4σ2-naphtho[1,8-cd ...
Stephanie F. Gait, Michael J. Rance, Charles W. Rees, Reginald W. Stephenson, Richard C. Storr   +4 more
openaire   +1 more source

1,11-Dipolar cycloaddition

Journal of the Chemical Society, Chemical Communications, 1972
2-Methylnaphtho[1,8-de]triazine undergoes 1,11-dipolar (12π+ 2π) cycloaddition to acetylenic esters to give 2-methylacenaphtho[5,6-de]triazines, after spontaneous dehydrogenation.
C. W. Rees, R. W. Stephenson, R. C. Storr   +2 more
openaire   +1 more source