.beta.-Hydride Elimination and Regioselectivity in the Rhodium-Catalyzed Hydroformylation of Open Chain Unsaturated Ethers

1995 ◽  
Vol 14 (10) ◽  
pp. 4644-4650 ◽  
Author(s):  
Raffaello Lazzaroni ◽  
Roberta Settambolo ◽  
Gloria Uccello-Barretta
Keyword(s):  
Open Chain ◽  
Beta Hydride Elimination ◽  
Hydride Elimination

.beta.-Hydride elimination from methoxo vs. ethyl ligands: thermolysis of (DPPE)Pt(OCH3)2, (DPPE)Pt(CH2CH3)(OCH3) and (DPPE)Pt(CH2CH3)2

1986 ◽  
Vol 108 (16) ◽  
pp. 4805-4813 ◽  
Author(s):  
Henry E. Bryndza ◽  
Joseph C. Calabrese ◽  
Marianne. Marsi ◽  
D. Christopher. Roe ◽  
Wilson. Tam ◽  
...  
Keyword(s):  
Beta Hydride Elimination ◽  
Hydride Elimination

Competitive uncatalyzed geometrical isomerization and .beta.-hydride elimination of alkyl complexes of platinum(II)

1989 ◽  
Vol 28 (2) ◽  
pp. 342-347 ◽  
Author(s):  
Giuseppe Alibrandi ◽  
Matteo Cusumano ◽  
Domenico Minniti ◽  
Luigi Monsu Scolaro ◽  
Raffaello Romeo
Keyword(s):  
Geometrical Isomerization ◽  
Alkyl Complexes ◽  
Beta Hydride Elimination ◽  
Hydride Elimination

Tertiary Alkylative Suzuki-Miyaura couplings

Synthesis ◽  
2022 ◽  
Author(s):  
Takashi Nishikata ◽  
Tom Sheppard ◽  
Naoki Tsuchiya
Keyword(s):  
Oxidative Addition ◽  
Short Review ◽  
The Other ◽  
Side Reactions ◽  
Coupling Reactions ◽  
Other Hand ◽  
Alkyl Electrophiles ◽  
Carbon Bonds ◽  
Beta Hydride Elimination ◽  
Hydride Elimination

The Suzuki-Miyaura coupling is extremely useful to construct Csp2-Csp2 carbon bonds. On the other hand, Csp2-Csp3 coupling reactions are do not work well, and tert-alkylative Suzuki-Miyaura coupling is particularly challenging due to problematic oxidative addition and beta-hydride elimination side reactions. In this short review, we will introduce recent examples of tert-alkylative Suzuki-Miyaura couplings with tert-alkyl electrophiles or -boron reagents. The review will mainly focus on catalyst and product structures and the proposed mechanisms .

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