In accessing trisubstituted vinyl boronates from terminal alkynes, a propargyl directing (2-pyridyl)sulfonyl group allows terminal alkynes to undergo Cu-catalyzed B2(pin)2-borylation and subsequent Cu-catalyzed allylic alkylation with Grignard reagents ...
Ramón Gómez Arrayás (1591966) +3 more
core +1 more source
Iron-Catalyzed Carboiodination of Alkynes
An iron-catalyzed carboiodination of alkynes with alkyl iodides at room temperature was developed. This method could provide synthetically useful vinyl iodides with general alkyl chains, fluoroalkyl group, ester, and cyano group.
Weili Deng +3 more
core +1 more source
Triethoxysilane-Catalyzed Sequential Regioselective Hydroboration of Terminal Alkynes: Sustainable Access to E-Alkenylboronate and Alkyl Gem-Diboronate Esters [PDF]
The commercial reagent, HSi(OEt)3, was an efficient catalyst for the synthesis of E-alkenylboronate esters and alkyl gem-diboronate esters by single or double hydroboration of terminal alkynes with HBPin (pinacolborane).
Himani, Ahuja +2 more
core +2 more sources
Gold(I) catalyzed hydroamination of alkenes and alkynes using hemilabile phosphine ligand
Au(PPO)Cl complex is a new gold catalyst which has been studied for hydrofunctionalizations of alkenes and alkynes. The bisphosphine monoxide is coordinated at the metal center as hemilabile ligand.
Immadi, Sri Sujana
core
Access to Indenones by Rhodium(III)-Catalyzed C-H Annulation of Arylnitrones with Internal Alkynes
Under redox-neutral conditions, rhodium(III)-catalyzed C-H annulation of N-tert-butyl-alpha-arylnitrones with internal alkynes has been realized for the synthesis of indenones under mild conditions.
李兴伟 +3 more
core +1 more source
Potential energy surfaces of gas-phased synchronous addition of HF to acetylene and methylacetylene. A non-empirical Harthree-Fock-Ruthane method (Gaussian-03, G-31++G** basis) with electronic correlation consideration in MP2 approximation (Moeller ...
Yu. B. Kirillov, N. M. Klimenko
doaj
Oxysulfonylation of Alkynes with Sodium Sulfinates to Access β-Keto Sulfones Catalyzed by BF3·OEt2
An efficient and operationally simple method for the synthesis of β-keto sulfones through the BF3·OEt2-promoted reaction of alkynes and sodium sulfinates is developed. With its facile and selective access to the targets, it features good functional group
Shi-Wei Yu +6 more
doaj +1 more source
Alkyne dichotomy and hydrogen migration in binuclear cyclopentadienylmetal alkyne complexes
Low-energy (Me 2 N) 2 C 2 M 2 (C 5 H 5 ) 2 (M = Ni ...
Huidong Li +9 more
openaire +2 more sources
Expanding Radical Chloropentafluorosulfanylation of Alkynes
The chloropentafluorosulfanylation of alkynes is a delicate but crucial operation for accessing SF5-alkynes that serve as substrates in numerous transformations. Dolbier’s procedure using Et3B/O2 was the most efficient approach, while recent efforts make
Thi Mo Nguyen (9378926) +5 more
core +1 more source
Synthesis and reactivity studies of mono- and diaurated species bearing N-heterocyclic carbene ligands [PDF]
The use of Au-NHC complexes in homogenous gold catalysis has become very popular during the last 10 years. The work described in this thesis represents a modest contribution towards a better understanding of the reactivity of these fascinating complexes ...
Gómez Suárez, Adrián
core

