One-Pot (3 + 2) Cycloaddition-Isomerization-Oxidation of 2,2,2-Trifluorodiazoethane and Styryl Derivatives. [PDF]
J Org Chem, 2023 Altarejos J +4 more
europepmc +1 more source
Computational study of the mechanism and selectivity of [3 + 2] cycloaddition reactions between nitrone and carbodiimide leading to the formation of anticancer 1,2,4-oxadiazolidine compounds from a MEDT perspective. [PDF]
Sci RepMellaoui MD +7 more
europepmc +1 more source
Furan Release via Force-Promoted Retro-[4+2][3+2] Cycloaddition. [PDF]
J Am Chem Soc, 2023 Suwada K, Ieong AW, Lo HLH, De Bo G.
europepmc +1 more source
Organocatalytic Asymmetric Formal Aza-[3 + 2] Cycloaddition via Domino Michael/Acetalization: Stereoselective Access to 3,4-<i>cis</i>-Disubstituted Pyrrolidines and Pot-Economical Total Syntheses of (-)-Kainic Acid and (-)-Domoic Acid. [PDF]
JACS AuHatano Y +3 more
europepmc +1 more source
Reaction profiles for quantum chemistry-computed [3 + 2] cycloaddition reactions. [PDF]
Sci Data, 2023 Stuyver T, Jorner K, Coley CW.
europepmc +1 more source
Photoredox catalytic asymmetric dearomative [3 + 2] cycloaddition of isoquinolines with enones. [PDF]
Nat CommunHuo J +5 more
europepmc +1 more source
On the Question of Zwitterionic Intermediates in the [3+2] Cycloaddition Reactions between Aryl Azides and Ethyl Propiolate. [PDF]
Molecules, 2023 Dresler E +3 more
europepmc +1 more source
Asymmetric [3 + 2] Cycloaddition to Access 3-Pyrrolines and Their Switchable Transformations to Nine-Membered Cyclic Sulfamidates and 2H-Pyrroles. [PDF]
Adv Sci (Weinh)Choi SM, Park JU, Kim JH.
europepmc +1 more source
Catalytic Asymmetric [3 + 2] Cycloaddition of Exocyclic Enol Ethers for the Synthesis of Spiroketals. [PDF]
Precis Chem, 2023 Zhang F +5 more
europepmc +1 more source
The high potential of methyl laurate as a recyclable competitor to conventional toxic solvents in [3 + 2] cycloaddition reactions. [PDF]
Beilstein J Org ChemYıldırım A, Göker M.
europepmc +1 more source