ChemInform Abstract: A Facile Synthesis of N-Carbamoylmethyl-α-aminobutyrolactones by the Ugi Multicomponent Condensation Reaction.

ChemInform ◽  
2010 ◽  
Vol 29 (50) ◽  
pp. no-no
Author(s):  
S. J. PARK ◽  
G. KEUM ◽  
S. B. KANG ◽  
H. Y. KOH ◽  
Y. KIM ◽  
...  
Keyword(s):  
Condensation Reaction ◽  
Facile Synthesis ◽  
Multicomponent Condensation

A facile synthesis of N-carbamoylmethyl- α -aminobutyrolactones by the Ugi multicomponent condensation reaction

1998 ◽  
Vol 39 (39) ◽  
pp. 7109-7112 ◽  
Author(s):  
Soo Jung Park ◽  
Gyochang Keum ◽  
Soon Bang Kang ◽  
Hun Yeong Koh ◽  
Youseung Kim ◽  
...  
Keyword(s):  
Condensation Reaction ◽  
Facile Synthesis ◽  
Multicomponent Condensation

Facile Synthesis of Nitrogen-Doped [(6.)m8]nCyclacene Carbon Nanobelts by a One-Pot Self-Condensation Reaction

2021 ◽  
Vol 143 (7) ◽  
pp. 2716-2721
Author(s):  
Jun Zhu ◽  
Yi Han ◽  
Yong Ni ◽  
Guangwu Li ◽  
Jishan Wu
Keyword(s):  
Condensation Reaction ◽  
Facile Synthesis ◽  
One Pot ◽  
Nitrogen Doped

Synthesis of β- and β,β-substituted Morita–Baylis–Hillman adducts using a two-step protocol

2012 ◽  
Vol 90 (5) ◽  
pp. 450-463 ◽  
Author(s):  
David I. Magee ◽  
Same Ratshonka ◽  
Jessica McConaghy ◽  
Maggie Hood
Keyword(s):  
Knoevenagel Condensation ◽  
Condensation Reaction ◽  
Facile Synthesis ◽  
Aliphatic Aldehydes ◽  
Tert Butyl ◽  
Keto Esters ◽  
Knoevenagel Condensation Reaction

The synthesis of a large number of β- and β,β-substituted keto esters was successful by the use of the Knoevenagel condensation reaction. The stereoselectivity of these reactions was improved by alteration of various substituent groups. Although there were few examples of complete Z selectivity, the use of tert-butyl acetoacetate with either aromatic or aliphatic aldehydes afforded Z selectivity. The selective reductions of these substituted keto esters was successfully achieved by using a combination of NaBH4 and CeCl3·7H2O or Yb(OTf)3, which allowed a facile synthesis of a large number of stereochemically pure substituted Morita–Baylis–Hillman adducts, including β,β-substituted adducts.

scholarly journals Facile synthesis of a semiconducting bithiophene-azine polymer and its application for organic thin film transistors and organic photovoltaics

RSC Advances ◽  
2020 ◽  
Vol 10 (22) ◽  
pp. 12876-12882
Author(s):  
Guanlin Wang ◽  
Pankaj Kumar ◽  
Zhifang Zhang ◽  
Arthur D. Hendsbee ◽  
Haitao Liu ◽  
...  
Keyword(s):  
Thin Film ◽  
Organic Photovoltaics ◽  
Thin Film Transistors ◽  
Printed Electronics ◽  
Condensation Reaction ◽  
Organic Thin Film Transistors ◽  
Organic Thin Film ◽  
Facile Synthesis

A new azine polymer poly(4,4′-didodecyl-2,2′-bithiophene-azine) (PDDBTA) is synthesized by a simple condensation reaction, which is a promising semiconductor for printed electronics.

Using the Ugi multicomponent condensation reaction to prepare families of chromophore appended azamacrocycles and their complexes

2008 ◽  
pp. 5212 ◽  
Author(s):  
Marcus Main ◽  
John S. Snaith ◽  
Marco M. Meloni ◽  
Maite Jauregui ◽  
Daniel Sykes ◽  
...  
Keyword(s):  
Condensation Reaction ◽  
Multicomponent Condensation

ChemInform Abstract: One-Pot Multicomponent Condensation Reaction of Aldehydes with Cyclic Ketones.

ChemInform ◽  
2011 ◽  
Vol 42 (32) ◽  
pp. no-no
Author(s):  
Ping Wu ◽  
Xi-Mei Cai ◽  
Qi-Fang Wang ◽  
Chao-Guo Yan
Keyword(s):  
Condensation Reaction ◽  
Cyclic Ketones ◽  
One Pot ◽  
Multicomponent Condensation

scholarly journals Solvent-free preparation of amidoalkyl phenols catalyzed by trityl chloride under neutral media

2015 ◽  
Vol 93 (11) ◽  
pp. 1245-1248 ◽  
Author(s):  
Ahmad Reza Moosavi-Zare ◽  
Mohammad Ali Zolfigol ◽  
Fateme Derakhshan-Panah ◽  
Masoume Daraei
Keyword(s):  
Condensation Reaction ◽  
Aromatic Aldehydes ◽  
Catalytic Amount ◽  
Solvent Free ◽  
One Pot ◽  
Multicomponent Condensation ◽  
Solvent Free Condition ◽  
Neutral Media ◽  
In Situ Generation

A one-pot, multicomponent condensation reaction of phenols, aromatic aldehydes, and amides in the presence of catalytic amount of trityl chloride as a homogeneous organocatalyst under solvent-free condition to prepare amidoalkyl phenols has been reported. It is interesting that trityl chloride by in situ generation of trityl carbocation with inherent instability catalyzes the reaction.

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