Heterogeneous-Gold-Catalyzed Acceptorless Cross-Dehydrogenative Coupling of Hydrosilanes and Isocyanic Acid Generated in situ from Urea

2013 ◽  
Vol 52 (32) ◽  
pp. 8420-8423 ◽  
Author(s):  
Kento Taniguchi ◽  
Shintaro Itagaki ◽  
Kazuya Yamaguchi ◽  
Noritaka Mizuno
2013 ◽  
Vol 125 (32) ◽  
pp. 8578-8581 ◽  
Author(s):  
Kento Taniguchi ◽  
Shintaro Itagaki ◽  
Kazuya Yamaguchi ◽  
Noritaka Mizuno

ChemInform ◽  
2013 ◽  
Vol 45 (1) ◽  
pp. no-no
Author(s):  
Kento Taniguchi ◽  
Shintaro Itagaki ◽  
Kazuya Yamaguchi ◽  
Noritaka Mizuno

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Chia-Yu Huang ◽  
Jianbin Li ◽  
Chao-Jun Li

AbstractHydrogen atom abstraction (HAT) from C(sp3)–H bonds of naturally abundant alkanes for alkyl radical generation represents a promising yet underexplored strategy in the alkylation reaction designs since involving stoichiometric oxidants, excessive alkane loading, and limited scope are common drawbacks. Here we report a photo-induced and chemical oxidant-free cross-dehydrogenative coupling (CDC) between alkanes and heteroarenes using catalytic chloride and cobalt catalyst. Couplings of strong C(sp3)–H bond-containing substrates and complex heteroarenes, have been achieved with satisfactory yields. This dual catalytic platform features the in situ engendered chlorine radical for alkyl radical generation and exploits the cobaloxime catalyst to enable the hydrogen evolution for catalytic turnover. The practical value of this protocol was demonstrated by the gram-scale synthesis of alkylated heteroarene with merely 3 equiv. alkane loading.


2019 ◽  
Vol 17 (20) ◽  
pp. 5121-5128 ◽  
Author(s):  
Fan Lv ◽  
Yang Yu ◽  
Erhong Hao ◽  
Changjiang Yu ◽  
Hua Wang ◽  
...  

An efficient protocol for the regioselective C–H α-formylation and α-acylation of BODIPY dyes using dioxolane derivatives as aldehyde equivalents is reported.


Synthesis ◽  
2021 ◽  
Author(s):  
Zongbin Jia ◽  
Qi Yang ◽  
Sanzhong Luo

We report herein a catalytic asymmetric dehydrogenative cross-coupling reaction between enones and tertiary amines enabled by synergistic photoredox and chiral primary amine catalysis. The reaction was proposed to proceed via the interception of iminium ion intermediate, in situ generated from photoredox oxidation, by dienamine at α-position, following by isomerization, leading to aza-Morita-Baylis-Hillman-type products with good diastereo- and enantio- selectivity.


2019 ◽  
Vol 59 (7) ◽  
pp. 31-36
Author(s):  
Ratmir R. Dashkin ◽  
◽  
Tatiana Yu. Vorobieva ◽  
Mary A. Seferyan ◽  
Daria V. Danilova ◽  
...  

A carbamates (urethanes) are an organic compounds with the general formula R'R''NCOOR are esters of carbamic acid and its derivatives. Due to their biological activity, carbamates are common as pesticides, insecticides, herbicides, and are used as drugs. Polyurethanes are widely used in industry. The main method of synthesis is the interaction of isocyanates with the corresponding alcohols or phenols, it is also possible to use urea, isocyanic acid or other methods, including the use of in-situ formed isocyanate. In the literature, N-alkyl-O-methylcarbamate is synthesized by reacting amines with dimethylcarbonates with various catalysts. In view of the economic feasibility and difficulty of isolating the target product the overwhelming number of the described methods are hardly applicable for scaling and industrial synthesis. A study was conducted to develop a method of synthesis of O-methyl-N-alkylcarbamate, which will be able to scale and be introduced into production. The most promising synthesis methods described in the literature have been tested, and a new method for producing various carbamates has been developed. The model amines for the experiment were selected industrially important – n-butylamine and cyclohexylamine. The structure of the product was confirmed by 1H NMR spectra. A number of the described methods had a way out in practice several times below the literature data presented, and some target products could not be received. The best way to react with n-butylamine is to use water as a catalyst. The yield obtained according to this procedure for O-methyl-N-cyclohexylcarbamate was 53%, for O-methyl-N-n-butylcarbamate – 68%, so the method was expanded to obtain several O-methyl-N-alkylcarbamate.


Synthesis ◽  
2019 ◽  
Vol 52 (01) ◽  
pp. 75-84 ◽  
Author(s):  
Peng Sun ◽  
Jiaojiao Yang ◽  
Zirui Song ◽  
Yichao Cai ◽  
Yajie Liu ◽  
...  

Starting from simple anilines and ester arylpropiolates, an efficient one-pot synthesis of 2-arylindole-3-carboxylate derivatives has been developed through copper-mediated sequential hydroamination and cross-dehydrogenative coupling (CDC) reaction. The initial hydroamination of anilines to ester arylpropiolates in benzene can proceed in a stereoselective manner to give ester (Z)-3-(arylamino)acrylates in the presence of CuCl2/phenanthroline, KMnO4, and KHCO3 at 120 °C. Sequentially, these in situ functionalized adducts can undergo direct intramolecular oxidative alkenylation of aromatic C–H bond in mixed solvents (benzene/DMSO 1:1) at 130 °C affording multi-substituted­ indoles in good to high yields.


2021 ◽  
Author(s):  
Halenur Özer ◽  
Dilan Arslan ◽  
Bengi Öztürk

In this study, in-situ formed ruthenium hydride species that were generated from Grubbs type catalyst are used as efficient catalysts for dehydrogenative alcohol coupling and sequential cross-metathesis/dehydrogenative coupling reactions. The...


2009 ◽  
Vol 48 (23) ◽  
pp. 10859-10861 ◽  
Author(s):  
Pei-Xiu Yin ◽  
Jian-Kai Cheng ◽  
Zhao-Ji Li ◽  
Lei Zhang ◽  
Ye-Yan Qin ◽  
...  

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