Results 161 to 170 of about 8,043 (225)

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

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

Recent advances of azomethine ylides for the synthesis of natural and synthetic bioactive pyrrolidines and spiropyrrolidines. [PDF]

RSC Adv
Paira P, Chakrabarty R, Deb Barman P, Singh B, Paira R.   +4 more
europepmc   +1 more source

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

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

Reactions of Nitrile Imines with Thiohydantoin Derivatives: Unexpected Chemoselectivity of the 1,3-Dipolar Cycloaddition: Preferential Addition of C=C rather than C=S Bonds. [PDF]

ACS Omega
Filkina ME, Zhukov EA, Tafeenko VA, Semykin AV, Kukushkin ME, Nechaev MS, Beloglazkina EK.   +6 more
europepmc   +1 more source

Ambident reactivity of enolizable 5-mercapto-1<i>H</i>-tetrazoles in trapping reactions with in situ-generated thiocarbonyl <i>S</i>-methanides derived from sterically crowded cycloaliphatic thioketones. [PDF]

Beilstein J Org Chem
Mlostoń G, Celeda M, Palusiak M, Heimgartner H, Denel-Bobrowska M, Olejniczak AB.   +5 more
europepmc   +1 more source

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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