Results 181 to 190 of about 153,572 (317)
Synthesis, Isolation, and Reactivity of a Phosphinidene Telluride
We describe the synthesis and isolation of a phosphinidene telluride. This species acts as a versatile phosphinidene transfer reagent accompanied by the extrusion of elemental tellurium. Abstract The synthesis and isolation of a phosphorus(III) telluride is reported.
Chenyang Hu +4 more
wiley +2 more sources
Recent Developments in Azomethine Ylide-Initiated Double Cycloadditions. [PDF]
Zhou T +4 more
europepmc +1 more source
Rhenium(I) tetrazylmethyl complexes serve as phosphorogenic bioorthogonal reagents, releasing luminescent and photocytotoxic rhenium(I) 3‐hydroxypyridine complexes and functional payloads upon reaction with 3‐isocyanopropyl derivatives. Their selective lysosomal accumulation in cancer cells and enhanced singlet oxygen photosensitization in acidic ...
Eunice Chiu‐Lam Mak +2 more
wiley +2 more sources
Cycloaddition and functionalization reactions involving tropone. [PDF]
Doraghi F +3 more
europepmc +1 more source
“Reverse-oriented” Cycloaddition of Nitrone to Enamine
Yujiro Nomura +2 more
openalex +1 more source
1,3-Dipolar Cycloadditions to Bicyclic Olefins. I. 1,3-Dipolar Cycloadditions to Norbornadienes [PDF]
Hisaji Taniguchi +3 more
openalex +1 more source
Silicon‐Based Azo Compound‐Mediated CO Activation and N2 Release
A rare silicon(IV)‐based azo compound featuring a Si─N═N─Si linkage was synthesized via the direct reaction of an organoazide with a silaiminyl–silylene precursor. This compound undergoes an unusual CO activation process, resulting in N2 release and complete cleavage of the C≡O bond, forming a Si(II)/Si(IV) product bridged by an oxygen atom and an ...
Da Jin +3 more
wiley +2 more sources
Total Synthesis of Calyciphylline F
The final challenge in the total synthesis of the caged polycyclic Daphniphyllum alkaloids was the Calyciphylline D‐type alkaloid, featuring a strained 8‐azatricyclo[4.2.1.04,8]nonane ring system. Presented herein is the total synthesis of calyciphylline F, a member of the calyciphylline D‐type alkaloid family, by an intramolecular [4 + 3 ...
Ryota Sato +5 more
wiley +2 more sources
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]
Filkina ME +6 more
europepmc +1 more source
A 1,3-Dipolar Cycloaddition and 1,3-Addition of 2-Methylfuran
L. FISERA +2 more
openalex +1 more source

