Results 81 to 90 of about 3,577 (190)
A cascade reaction under phase‐transfer conditions between 3‐nitro indoles and isocyanomethylene dibenzenes affords the construction of pyrrolo[3,4‐b]indole cores. Control experiments provide insight into moderate product yields and clarify why the reaction is not amenable to asymmetric induction. A cascade reaction enabling the construction of pyrrolo[
Ana Mikleušević +4 more
wiley +1 more source
1,2,4‐Oxadiazole[4,5‐a]piridinium salts add alcohols and alkoxides to undergo electrocyclic ring opening affording alkoxybutadienyl 1,2,4‐oxadiazole derivatives.
Dr. Mattia Moiola +2 more
doaj +1 more source
Enantioselective 1,3-Dipolar Cycloadditions of α-Methylene Lactams to Construct Spirocycles. [PDF]
Nishiura Y +3 more
europepmc +1 more source
Phospha-Münchnones: Electronic Structures and 1,3-Dipolar Cycloadditions
The reaction of imines, acid chlorides, PR3, and base generates a new class of 1,3-dipoles: phospha-Münchnones. These 1,3-dipoles can undergo cycloadditions with alkynes followed by loss of phosphine oxides to form pyrroles.
Bruce A. Arndtsen (1310721) +5 more
core +2 more sources
An Overlooked Pathway in 1,3-Dipolar Cycloadditions of Diazoalkanes with Enamines. [PDF]
Li L +5 more
europepmc +1 more source
Photocatalytic (3 + 2) dipolar cycloadditions of aziridines driven by visible-light. [PDF]
Mazzarella D +3 more
europepmc +1 more source
Dynamic Catalytic Highly Enantioselective 1,3-Dipolar Cycloadditions. [PDF]
Yildirim O +5 more
europepmc +1 more source
Trimethylsilyldiazomethane (TMS-CHN2) reacts readily with hetaryl thioketones to give sterically crowded 2-trimethylsilyl-4,4,5,5-tetrahetaryl-1,3-dithiolanes with complete regioselectivity at −75 °C as well as at rt.
Grzegorz Mlostoń +3 more
doaj +1 more source
Catalytic Enantioselective 1,3-Dipolar Cycloadditions between Nitrones and Alkenes Using a Novel Heterochiral Ytterbium(III ...
Shū Kobayashi (2450098) +1 more
core +1 more source
SuFExable NH-Pyrazoles via 1,3-Dipolar Cycloadditions of Diazo Compounds with Bromoethenylsulfonyl Fluoride. [PDF]
Yamanushkin P +3 more
europepmc +1 more source

