Results 251 to 260 of about 70,860 (329)

Electrophilic Functionalization of Donor‐Stabilized Phosphanylboranes: A New Pathway toward Heavy 13/14/15 Parent Hydride‐Containing Compounds

open access: yesChemistryEurope, EarlyView.
A new way of obtaining mixed 13/14/15 hydride containing compounds stabilized only by a Lewis base is presented. The functionalization of IDipp·BH2PH2 (IDipp = 1,3‐Bis‐(2,6‐diisopropylphenyl)‐imidazolin‐2‐ylidene) by main group electrophiles leads to the formation of the compounds [IDipp·BH2PH2E]+ [E = H, CH3 SiEt3, Ge(SiMe3)3, SnMe3) which represent a
Robert Szlosek   +7 more
wiley   +1 more source

Skeletal Editing from Pyridine to Aniline via C‐Insertion and N‐Isomerization

open access: yesChemistryEurope, EarlyView.
A concise protocol is presented that converts pyridines into anilines by externalizing the original pyridine nitrogen at either the "ipso" or "ortho" position, which results in para or meta‐primary aniline products. A key carbene‐insertion step precedes nitrogen migration, preserving both ring size and overall structure.
Yun Luo   +3 more
wiley   +1 more source

Rapidly diastereoselective assembly of ten-membered N-heterocycles between two 1,3-dipoles and their diversity to access fused N-heterocycles

open access: hybrid
Yan Luo   +8 more
openalex   +1 more source

Enantioselective Synthesis of Sulfinamidines via Asymmetric Rhodium–Catalyzed Imidation of Sulfenamides

open access: yesChemistryEurope, EarlyView.
In this work, a catalytic enantioselective imidation approach is presented for the preparation of enantioenriched sulfinamidines from sulfenamides, employing a chiral dirhodium(II) tetracarboxylate catalyst. This method enables the imidation of N,N‐bisalkyl sulfenamides in yields of up to 98% and enantiomeric ratios up to 98:2, with a catalyst loading ...
Michael Andresini   +7 more
wiley   +1 more source

[3 + 2] Cycloaddition of thioformylium methylide with various arylidene-azolones in the synthesis of 7-thia-3-azaspiro[4.4]nonan-4-ones. [PDF]

open access: yesBeilstein J Org Chem
Rudik DI   +7 more
europepmc   +1 more source

Bis‐Dichlorosilyl Functionalized C4‐Cumulene With Unique Bonding Scenario

open access: yesChemistry – A European Journal, EarlyView.
Herein, we report a silylene‐functionalized C4‐cumulene (2) and investigate its bonding scenario employing computational methods such as NBO analysis, AIM, and energy decomposition analysis‐natural orbital for chemical valence (EDA‐NOCV). The EDA‐NOCV analysis showed that compound 2 prefers to possess electron‐sharing covalent sigma and dative covalent
Saroj Kumar Kushvaha   +10 more
wiley   +1 more source

Home - About - Disclaimer - Privacy