One-pot synthesis of hyperbranched poly(amido amine) clicked with a sugar shell via Michael addition polymerization and thiol click reaction

2010 ◽  
Vol 53 (8) ◽  
pp. 1663-1668 ◽  
Author(s):  
ZhiQiang Yu ◽  
MengMeng Cui ◽  
JunJie Yan ◽  
YeZi You
Keyword(s):  
Michael Addition ◽  
Click Reaction ◽  
One Pot ◽  
One Pot Synthesis ◽  
Addition Polymerization ◽  
Hyperbranched Poly ◽  
Michael Addition Polymerization

Synthesis of Thermoresponsive Nonconjugated Fluorescent Branched Poly(ether amide)s via Oxa-Michael Addition Polymerization

2021 ◽  
Author(s):  
Qimin Jiang ◽  
Liang Zhao ◽  
Yongzhuang Du ◽  
Wenyan Huang ◽  
Xiaoqiang Xue ◽  
...  
Keyword(s):  
Michael Addition ◽  
Biological Applications ◽  
Stimuli Responsive ◽  
One Pot ◽  
One Pot Synthesis ◽  
Addition Polymerization ◽  
Straightforward Method ◽  
Fluorescent Polymers ◽  
The One ◽  
Michael Addition Polymerization

With the aim of providing a straightforward method for the synthesis of stimuli-responsive nonconjugated fluorescent polymers suitable for biological applications, this study describes the one-pot synthesis of novel thermoresponsive nonconjugated...

Facile one-pot synthesis of novel water-soluble fluorescent hyperbranched poly(amino esters)

RSC Advances ◽  
2016 ◽  
Vol 6 (91) ◽  
pp. 88030-88037 ◽  
Author(s):  
Yuqun Du ◽  
Hongxia Yan ◽  
Song Niu ◽  
Lihua Bai ◽  
Fu Chai
Keyword(s):  
Michael Addition ◽  
Addition Reaction ◽  
Water Soluble ◽  
Michael Addition Reaction ◽  
One Pot ◽  
Amino Esters ◽  
One Pot Synthesis ◽  
Hyperbranched Poly ◽  
Trimethylolpropane Triacrylate ◽  
Aliphatic Diamines

Two kinds of water-soluble fluorescent hyperbranched poly(amino esters) were first synthesized by a convenient one-pot approach via the A2 + B3 Michael addition reaction of trimethylolpropane triacrylate and aliphatic diamines.

Catalyst-Free One-Pot Synthesis of Novel Heteroarylamine Substituted Furo[3,2-c]coumarins

Synlett ◽  
2018 ◽  
Vol 29 (12) ◽  
pp. 1589-1592 ◽  
Author(s):  
Abolfazl Olyaei ◽  
Mahnaz Saraei ◽  
Reyhaneh Khoeiniha
Keyword(s):  
Michael Addition ◽  
Aldol Condensation ◽  
Ring Closure ◽  
Dehydration Reaction ◽  
One Pot ◽  
Catalyst Free ◽  
One Pot Synthesis ◽  
Tandem Process ◽  
First Time

A high-yielding cyclocondensation of 4-hydroxycoumarin, phenylglyoxal monohydrate, and heteroarylamines proceeds without catalysis, which gives novel functionalized furo[3,2-c]coumarins and heteroarylamino alkylation of coumarin products in acetonitrile under reflux, is reported for the first time. This tandem process involves sequentially an aldol condensation, Michael addition, a ring closure, and dehydration reaction.

One-Pot Synthesis of Highly Substituted Allenylidene Derivatives via Palladium- or Nickel-Catalyzed Tandem Michael Addition-Cyclization Reaction

2009 ◽  
Vol 351 (1-2) ◽  
pp. 141-146 ◽  
Author(s):  
Yun Shi ◽  
Jing Huang ◽  
Yan-Fang Yang ◽  
Lu-Yong Wu ◽  
Yan-Ning Niu ◽  
...  
Keyword(s):  
Michael Addition ◽  
Cyclization Reaction ◽  
One Pot ◽  
One Pot Synthesis
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