One-Pot Three-Step Polymerization System Using Double Click Michael Addition and Radical Photopolymerization

We present the first xanthate surface functional dendrimers which undergo rapid one-pot deprotection to thiols and subsequent acrylate Michael addition .

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

Synlett ◽

10.1055/s-0036-1591582 ◽

2018 ◽

Vol 29 (12) ◽

pp. 1589-1592 ◽

Cited By ~ 6

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.

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

Advanced Synthesis & Catalysis ◽

10.1002/adsc.200800582 ◽

2009 ◽

Vol 351 (1-2) ◽

pp. 141-146 ◽

Cited By ~ 19

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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Uncatalyzed diastereoselective synthesis of alkyliminofurochromone-derived benzylmalononitriles via a three-component cascade reaction: competition between Diels–Alder cycloaddition and Michael addition

Organic & Biomolecular Chemistry ◽

10.1039/d0ob02540b ◽

2021 ◽

Author(s):

Mohammad Bagher Teimouri ◽

Zahra Mokhtare ◽

Hamid Reza Khavasi

Keyword(s):

Michael Addition ◽

Heterocyclic Ring ◽

Cascade Reaction ◽

Diels Alder ◽

Chemical Bonds ◽

Diastereoselective Synthesis ◽

Atom Economy ◽

One Pot

Three new chemical bonds and three stereogenic centres and one heterocyclic ring were assembled stereoselectively in a convenient high atom-economy one-pot operation.

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Regio- and Stereoselective One-Pot Synthesis of Unknown Oxazoline-Fused Pyridazines by ‘Michael Addition-Pyridazine Cyclization-Oxazoline Cyclization’ Cascade Reactions of 4-Chloro-1,2-diaza-1,3-butadienes with 3-Dimethylaminopropenoates

Synlett ◽

10.1055/s-2007-990962 ◽

2007 ◽

Vol 2007 (19) ◽

pp. 2971-2974 ◽

Cited By ~ 18

Author(s):

Orazio Attanasi ◽

Gianfranco Favi ◽

Paolino Filippone ◽

Amalija Golobič ◽

Francesca Perrulli ◽

...

Keyword(s):

Michael Addition ◽

Cascade Reactions ◽

One Pot ◽

One Pot Synthesis

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ChemInform Abstract: One-Pot Three-Component Syntheses of Indoloquinolizidine Derivatives Using an Organocatalytic Michael Addition and Subsequent Pictet-Spengler Cyclization.

ChemInform ◽

10.1002/chin.201207141 ◽

2012 ◽

Vol 43 (7) ◽

pp. no-no

Author(s):

Xiaoyu Wu ◽

Xiaoyang Dai ◽

Huihui Fang ◽

Linlin Nie ◽

Jie Chen ◽

...

Keyword(s):

Michael Addition ◽

One Pot

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One-pot organocatalytic enantioselective Michael addition and aza-cyclization/dehydration cascade reaction strategy: asymmetric synthesis of highly functionalized 1,4-dihydroquinolines

Tetrahedron Letters ◽

10.1016/j.tetlet.2015.06.071 ◽

2015 ◽

Vol 56 (33) ◽

pp. 4819-4823 ◽

Cited By ~ 15

Author(s):

Hanna Kim ◽

Sung-Gon Kim

Keyword(s):

Asymmetric Synthesis ◽

Michael Addition ◽

Cascade Reaction ◽

One Pot

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Efficient Synthesis of 3-Amino-1,5-benzodiazepine-2-one Derivatives

Synlett ◽

10.1055/s-0036-1588954 ◽

2017 ◽

Vol 28 (10) ◽

pp. 1183-1186 ◽

Cited By ~ 4

Author(s):

Nobuhiro Obara ◽

Takeshi Watanabe ◽

Tomohiro Asakawa ◽

Toshiyuki Kan ◽

Takao Tanaka

Keyword(s):

Michael Addition ◽

Convenient Method ◽

Addition Reaction ◽

Efficient Synthesis ◽

Michael Addition Reaction ◽

One Pot ◽

Simple Method ◽

The Michael Addition

A convenient method for synthesizing 3-amino-1,5-benzodiazepine-2-one via the Michael addition reaction of o-phenylenediamine with dehydroalanine ester derivatives, followed by cyclization, was developed. This simple method was used to obtain a variety of N-substituted 3-amino-1,5-benzodiazepine-2-ones in one pot with good yields.

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