One-Pot Synthesis of Cycloocta[b ]indole Through Formal [5+3] Cycloaddition Using Donor-Acceptor Cyclopropanes

2019 ◽  
Vol 2019 (24) ◽  
pp. 3916-3920 ◽  
Author(s):  
Akito Okabe ◽  
Shinji Harada ◽  
Takuya Takeda ◽  
Atsushi Nishida
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Donor Acceptor

ChemInform Abstract: A Convenient Tandem One-Pot Synthesis of Donor-Acceptor-Type Triphenylene 2,3-Dicarboxylic Esters from Diarylacetylene.

ChemInform ◽  
2015 ◽  
Vol 46 (8) ◽  
pp. no-no
Author(s):  
Chun Feng ◽  
Xian-Li Tian ◽  
Jing Zhou ◽  
Shi-Kai Xiang ◽  
Wen-Hao Yu ◽  
...  
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Donor Acceptor

One-Pot Synthesis and Characterization of a Chromophore−Donor−Acceptor Assembly

2000 ◽  
Vol 39 (1) ◽  
pp. 71-75 ◽  
Author(s):  
Kimberly A. Maxwell ◽  
Milan Sykora ◽  
Joseph M. DeSimone ◽  
Thomas J. Meyer
Keyword(s):  
Synthesis And Characterization ◽  
One Pot ◽  
One Pot Synthesis ◽  
Donor Acceptor

scholarly journals Efficient Straightforward Synthesis of Amidopiperazinophanes as Versatile Novel Supramolecular Scaffolds

SynOpen ◽  
2019 ◽  
Vol 03 (04) ◽  
pp. 157-163
Author(s):  
Ayyavu Thirunarayanan ◽  
Sivasamy Selvarani ◽  
Gracia Francisco ◽  
Perumal Rajakumar
Keyword(s):  
Electron Donor ◽  
Multicomponent Reaction ◽  
Mannich Reaction ◽  
One Pot ◽  
One Pot Synthesis ◽  
Supramolecular Scaffolds ◽  
Donor Acceptor ◽  
The Mannich Reaction

A simple one-pot synthesis of amidopiperazinophanes with a combination of electron-deficient amide groups and electron-rich alkyne and piperazine functionalities has been achieved by using multicomponent reaction (MCR) methodology with the Mannich reaction. Herein, we demonstrate the synthesis of macrocyclic amide structures in good yields. These macrocycles, with electron donor/acceptor sites, are versatile molecules for host–guest and binding.

scholarly journals One-pot synthesis of GABA amides via the nucleophilic addition of amines to 3,3-disubstituted cyclopropenes

2015 ◽  
Vol 13 (34) ◽  
pp. 8993-8995 ◽  
Author(s):  
Vladimir A. Maslivetc ◽  
Marina Rubina ◽  
Michael Rubin
Keyword(s):  
Double Bond ◽  
Nucleophilic Addition ◽  
Ring Opening ◽  
Secondary Amines ◽  
One Pot ◽  
One Pot Synthesis ◽  
Primary And Secondary Amines ◽  
Donor Acceptor

A one-pot synthesis of various GABA amides has been demostrated, employing the nucleophilic addition of primary and secondary amines across the double bond of cyclopropene-3-carboxamides, followed by ring-opening of the resulting donor–acceptor cyclopropanes and subsequent in situ reduction of enamine intermediates.

One-pot synthesis of 2-bromo-4,5-diazafluoren-9-one via a tandem oxidation–bromination-rearrangement of phenanthroline and its hammer-shaped donor–acceptor organic semiconductors

Tetrahedron ◽  
2011 ◽  
Vol 67 (10) ◽  
pp. 1977-1982 ◽  
Author(s):  
Jian-Feng Zhao ◽  
Lin Chen ◽  
Peng-Ju Sun ◽  
Xiao-Ya Hou ◽  
Xiang-Hua Zhao ◽  
...  
Keyword(s):  
Organic Semiconductors ◽  
One Pot ◽  
One Pot Synthesis ◽  
Donor Acceptor

One-pot synthesis of donor–acceptor [2]rotaxanes based on cryptand–paraquat recognition motif

2011 ◽  
Vol 9 (4) ◽  
pp. 1237 ◽  
Author(s):  
Zhikai Xu ◽  
Lasheng Jiang ◽  
Yahui Feng ◽  
Suhui Zhang ◽  
Jidong Liang ◽  
...  
Keyword(s):  
One Pot ◽  
Recognition Motif ◽  
One Pot Synthesis ◽  
Donor Acceptor

scholarly journals A convenient tandem one-pot synthesis of donor–acceptor-type triphenylene 2,3-dicarboxylic esters from diarylacetylene

2014 ◽  
Vol 12 (36) ◽  
pp. 6977-6981 ◽  
Author(s):  
Chun Feng ◽  
Xian-Li Tian ◽  
Jing Zhou ◽  
Shi-Kai Xiang ◽  
Wen-Hao Yu ◽  
...  
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Synthetic Procedure ◽  
Donor Acceptor ◽  
Direct Preparation

An efficient one-pot synthetic procedure was developed for the direct preparation of polysubstituted triphenylene 2,3-dicarboxylic esters via a tandem addition process from diarylacetylene.

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