Gold Sulfonium Benzylide Complexes Undergo Efficient Benzylidene Transfer to Alkenes
Autor: | Ross A. Widenhoefer, Robert G. Carden |
---|---|
Rok vydání: | 2019 |
Předmět: |
chemistry.chemical_classification
Trifluoromethyl Sulfide 010405 organic chemistry Sulfonium Sodium Organic Chemistry Kinetics Cationic polymerization chemistry.chemical_element General Chemistry 010402 general chemistry 01 natural sciences Medicinal chemistry Catalysis 0104 chemical sciences Styrene chemistry.chemical_compound chemistry Boron |
Zdroj: | Chemistry – A European Journal. 25:11026-11030 |
ISSN: | 1521-3765 0947-6539 |
DOI: | 10.1002/chem.201902845 |
Popis: | The gold sulfonium benzylide complexes [(P1)AuCHPh(SR1 R2 )]+ {B[3,5-CF3 C6 H3 ]4 }- [P1=P(tBu)2 o-biphenyl; R1 , R2 =-(CH2 )4 - (1 a); R1 =Et, R2 =Ph (1 b); R1 =R2 =Ph (1 c)] were synthesized by reaction of the gold α-chloro benzyl complex (P1)AuCHClPh with sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate and excess sulfide. Complexes 1 undergo efficient benzylidene transfer to alkenes and DMSO under mild conditions without external activation. Kinetic analysis of the reaction of 1 c with styrene was consistent with the intermediacy of the cationic gold benzylidene complex [(P1)AuCHPh]+ (I). |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |