Enantiodivergent One‐Pot Synthesis of Axially Chiral Biaryls Using Organocatalyst‐Mediated Enantioselective Domino Reaction and Central‐to‐Axial Chirality Conversion

2021 ◽  
Author(s):  
Seitaro Koshino ◽  
Tohru Taniguchi ◽  
Kenji Monde ◽  
Eunsang Kwon ◽  
Yujiro Hayashi
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
Axial Chirality ◽  
One Pot Synthesis ◽  
Axially Chiral

Synthesis of pyrazolo[1,5-c]quinazoline derivatives through the copper-catalyzed domino reaction of o-alkenyl aromatic isocyanides with diazo compounds

2020 ◽  
Vol 56 (55) ◽  
pp. 7665-7668 ◽  
Author(s):  
Lu Liu ◽  
Lei Li ◽  
Shukuan Mao ◽  
Xin Wang ◽  
Ming-Dong Zhou ◽  
...  
Keyword(s):  
Diazo Compounds ◽  
Domino Reaction ◽  
Reaction Conditions ◽  
One Pot ◽  
One Pot Synthesis ◽  
Quinazoline Derivatives

Various o-alkenyl aromatic isocyanides were prepared from readily available reactants for their double annulation with diazo compounds for a one-pot synthesis of pyrazolo[1,5-c]quinazolines under mild reaction conditions.

ChemInform Abstract: Palladium-Catalyzed Intermolecular Domino Reaction of gem-Dibromoenynes with Anilines: A One-Pot Synthesis of Quinolines and Quinolinones.

ChemInform ◽  
2012 ◽  
Vol 43 (51) ◽  
pp. no-no
Author(s):  
Tianhao Meng ◽  
Wen-Xiong Zhang ◽  
Hui-Jun Zhang ◽  
Yun Liang ◽  
Zhenfeng Xi
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
One Pot Synthesis ◽  
Palladium Catalyzed

One-Pot Synthesis of Highly Substituted 4-Acetonylindoles via Sequential Dearomatization and Silver-Catalyzed Domino Reaction

2014 ◽  
Vol 16 (13) ◽  
pp. 3600-3603 ◽  
Author(s):  
Xin Feng ◽  
Huiqing Wang ◽  
Bo Yang ◽  
Renhua Fan
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
One Pot Synthesis

ChemInform Abstract: A Novel and Efficient Domino Reaction for the One-Pot Synthesis of Spiro-2-aminopyrimidinones.

ChemInform ◽  
2008 ◽  
Vol 39 (40) ◽  
Author(s):  
Sorour Ramezanpour ◽  
Mehri Seyed Hashtroudi ◽  
Hamid Reza Bijanzadeh ◽  
Saeed Balalaie
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One

A new ‘one-pot’ synthesis of 2-substituted 3-nitro pyrrolidines through a multicomponent domino reaction

2004 ◽  
Vol 45 (7) ◽  
pp. 1373-1375 ◽  
Author(s):  
Nikla Baricordi ◽  
Simonetta Benetti ◽  
Gisella Biondini ◽  
Carmela De Risi ◽  
Gian P. Pollini
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
One Pot Synthesis

IBX-promoted domino reaction of α-hydroxy amides: a facile one-pot synthesis of isatins

RSC Advances ◽  
2016 ◽  
Vol 6 (4) ◽  
pp. 2870-2874 ◽  
Author(s):  
Yaoling Wang ◽  
Xu Cheng ◽  
Zhen Zhan ◽  
Xiaojun Ma ◽  
Ruifang Nie ◽  
...  
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
One Pot Synthesis ◽  
Temperature Controlled

A novel and temperature-controlled oxidation of α-hydroxy amides in the presence of IBX is described.

ChemInform Abstract: IBX-Promoted Domino Reaction of α-Hydroxy Amides: A Facile One-Pot Synthesis of Isatins.

ChemInform ◽  
2016 ◽  
Vol 47 (21) ◽  
Author(s):  
Yaoling Wang ◽  
Xu Cheng ◽  
Zhen Zhan ◽  
Xiaojun Ma ◽  
Ruifang Nie ◽  
...  
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
One Pot Synthesis

scholarly journals Homochiral BINOL-based macrocycles with π-electron-rich, electron-withdrawing or extended spacing units as receptors for C60

2014 ◽  
Vol 10 ◽  
pp. 1308-1316 ◽  
Author(s):  
Marco Caricato ◽  
Silvia Díez González ◽  
Idoia Arandia Ariño ◽  
Dario Pasini
Keyword(s):  
Dicarboxylic Acids ◽  
Spectroscopic Methods ◽  
Statistical Distributions ◽  
One Pot ◽  
Enantiomerically Pure ◽  
One Pot Synthesis ◽  
Axially Chiral ◽  
Aromatic Dicarboxylic Acids ◽  
The One ◽  
Cyclic Adducts

The “one-pot” synthesis of several homochiral macrocycles has been achieved by using π-electron-rich, electron-deficient or extended aromatic dicarboxylic acids in combination with an axially-chiral dibenzylic alcohol, derived from enantiomerically-pure BINOL. Two series of cyclic adducts with average molecular D 2 and D 3 molecular symmetries, respectively, have been isolated in pure forms. Their yields and selectivities deviate substantially from statistical distributions. NMR and CD spectroscopic methods are efficient and functional in order to highlight the variability of shapes of the covalent macrocyclic frameworks. The larger D 3 cyclic adducts exhibit recognition properties towards C60 in toluene solutions (up to log K a = 3.2) with variable stoichiometries and variable intensities of the charge-tranfer band upon complexation.

Facile One-pot Synthesis of Substituted Dihydropyrrol-2-onesviaFour-component Domino Reaction of Amines, Dialkyl Acetylenedicarboxylates and Formaldehyde

2013 ◽  
Vol 60 (8) ◽  
pp. 1003-1006 ◽  
Author(s):  
Seyed Sajad Sajadikhah ◽  
Nourallah Hazeri ◽  
Malek Taher Maghsoodlou ◽  
Sayyed Mostafa Habibi-Khorassani
Keyword(s):  
Domino Reaction ◽  
One Pot ◽  
Dialkyl Acetylenedicarboxylates ◽  
One Pot Synthesis
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