“One pot” and selective synthesis of monoglycerides over homogeneous and heterogeneous guanidine catalysts

2004 ◽  
Vol 6 (2) ◽  
pp. 72-74 ◽  
Author(s):  
François Jérôme ◽  
Ghizlane Kharchafi ◽  
Isabelle Adam ◽  
Joël Barrault
Keyword(s):  
ChemInform ◽  
2009 ◽  
Vol 40 (42) ◽  
Author(s):  
Ren-Jie Song ◽  
Yu Liu ◽  
Rong-Jiang Li ◽  
Jin-Heng Li
Keyword(s):  

2009 ◽  
Vol 87 (6) ◽  
pp. 698-705 ◽  
Author(s):  
Nagarajan Panneer Selvam ◽  
Paramasivan T. Perumal

A convenient and diastereoselective one-pot synthesis of cis-4-amidotetrahydropyrans is described. This simple protocol involves Prins cyclization of homoallylic alcohol and aldehydes, followed by Ritter reaction of acetonitrile leading to the formation of cis-4-acetamidopyrans in good yields.


Tetrahedron ◽  
2016 ◽  
Vol 72 (44) ◽  
pp. 7070-7075 ◽  
Author(s):  
Abdolali Alizadeh ◽  
Akram Bagherinejad ◽  
Fahimeh Bayat ◽  
Long-Guan Zhu
Keyword(s):  

Tetrahedron ◽  
2016 ◽  
Vol 72 (8) ◽  
pp. 1051-1057 ◽  
Author(s):  
Sheng-Rong Liao ◽  
Li-Juan Du ◽  
Xiao-Chu Qin ◽  
Liang Xu ◽  
Jun-Feng Wang ◽  
...  

2008 ◽  
Vol 49 (23) ◽  
pp. 3814-3818 ◽  
Author(s):  
Jiuxi Chen ◽  
Dengze Wu ◽  
Fei He ◽  
Miaochang Liu ◽  
Huayue Wu ◽  
...  
Keyword(s):  

2014 ◽  
Vol 10 ◽  
pp. 26-33 ◽  
Author(s):  
Samir Kundu ◽  
Babli Roy ◽  
Basudeb Basu

The development of a silica-promoted highly selective synthesis of 1,2 or 1,3-dithioethers via solvent-free one-pot tandem reactions of an allyl bromide with excess thiol at room temperature is described. The choice of silica gel, either pre-calcined or moistened with water, exhibited notable regioselectivity in the formation of dithioethers. Plausible mechanistic routes were explored and postulated.


RSC Advances ◽  
2014 ◽  
Vol 4 (42) ◽  
pp. 21765-21771 ◽  
Author(s):  
Ren-Jian Wei ◽  
Ying-Ying Zhang ◽  
Xing-Hong Zhang ◽  
Bin-Yang Du ◽  
Zhi-Qiang Fan

This work describes the first regio-selective synthesis of poly(epichlorohydrin) diol via a simple one-pot bulk polymerization with a heterogeneous catalyst.


2015 ◽  
Vol 87 (9-10) ◽  
pp. 1011-1019 ◽  
Author(s):  
Armando Córdova

AbstractThe interplay and synergistic cooperation between homogeneous and heterogeneous catalyst systems is of utmost importance in nature. It is also applied in chemical synthesis. Here, it can allow for new reactivity, which is not possible by the employment of a single catalyst, and promote the catalysis of multiple transformations in a one-pot sequence. This could overall lead to novel reactions and the development of sustainable chemistry. In this context, a versatile and broad synergistic strategy for the selective synthesis of valuable molecules with variable complexity and under eco-friendly conditions is disclosed. It is based on integrated heterogeneous metal/organo multiple relay catalysis, which is performed in a single reaction vessel, and allows for the assembly of complex molecules (e.g., heterocycles and carbocycles) with up to three quaternary stereocenters in a highly enantioselective fashion from simple alcohols and air/O2.


2019 ◽  
Vol 2019 (36) ◽  
pp. 6240-6245
Author(s):  
Svetlana F. Malysheva ◽  
Vladimir A. Kuimov ◽  
Natalia A. Belogorlova ◽  
Alexander I. Albanov ◽  
Nina K. Gusarova ◽  
...  

2019 ◽  
Vol 15 ◽  
pp. 378-387
Author(s):  
Adrián A Heredia ◽  
Martín G López-Vidal ◽  
Marcela Kurina-Sanz ◽  
Fabricio R Bisogno ◽  
Alicia B Peñéñory

A preparation of β-ketosulfides avoiding the use of thiols is described. The combination of a multicomponent reaction and a lipase-catalysed hydrolysis has been developed in order to obtain high chemical diversity employing a single sulfur donor. This methodology for the selective synthesis of a set of β-ketosulfides is performed under mild conditions and can be set up in one-pot two-step and on a gram-scale.


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