One-pot sequential reaction to 2-substituted-phenanthridinones from N-methoxybenzamides

2017 ◽  
Vol 15 (20) ◽  
pp. 4390-4398 ◽  
Author(s):  
Dongdong Liang ◽  
Deanna Sersen ◽  
Chao Yang ◽  
Jeffrey R. Deschamps ◽  
Gregory H. Imler ◽  
...  
Keyword(s):  
Hypervalent Iodine ◽  
One Pot ◽  
Sequential Reaction ◽  
One Pot Synthesis ◽  
Halogenation Reaction

A one-pot synthesis of 2-bromo/chloro-phenanthridinones via an amidation of arenes followed by a regioselective halogenation reaction has been developed using a hypervalent iodine reagent.

Hypervalent-Iodine Mediated One-Pot Synthesis of Isoxazolines and Isoxazoles bearing Difluoromethyl Phosphonate Moiety

2021 ◽  
Author(s):  
Romana Pajkert ◽  
Henryk Koroniak ◽  
Pawel Kafarski ◽  
Gerd Volker Roeschenthaler
Keyword(s):  
Nitrile Oxide ◽  
Dipolar Cycloaddition ◽  
Hypervalent Iodine ◽  
One Pot ◽  
One Pot Synthesis

A one-pot, regioselective 1,3-dipolar cycloaddition of in situ generated (diethoxyphosphoryl)difluoromethyl nitrile oxide toward selected alkenes and alkynes is reported. This protocol enables facile access to 3,5-disubstituted isoxazolines and isoxazoles bearing...

One-pot synthesis of 6,11-dihydro-5H-indolizino[8,7-b]indoles via sequential formation of β-enamino ester, Michael addition and Pictet–Spengler reactions

RSC Advances ◽  
2014 ◽  
Vol 4 (108) ◽  
pp. 62817-62826 ◽  
Author(s):  
Dan Zhu ◽  
Jing Sun ◽  
Chao-Guo Yan
Keyword(s):  
Michael Addition ◽  
One Pot ◽  
Sequential Reaction ◽  
One Pot Synthesis ◽  
Sequential Formation

One pot sequential reaction of generation of β-enamino ester, Michael addition and Pictet–Spengler reaction.

One-Pot Syntheses of Diaryliodonium Salts from Aryl Iodides Using Peracetic Acid as Green Oxidant

2011 ◽  
Vol 64 (5) ◽  
pp. 529 ◽  
Author(s):  
Toshifumi Dohi ◽  
Nobutaka Yamaoka ◽  
Itsuki Itani ◽  
Yasuyuki Kita
Keyword(s):  
Peracetic Acid ◽  
Hypervalent Iodine ◽  
One Pot ◽  
Iodine Species ◽  
One Pot Synthesis ◽  
Diaryliodonium Salts ◽  
Aryl Iodides ◽  
First Time

The rate-accelerating effects of fluoroalcohol solvents for generating trivalent hypervalent iodine species and the conversion into diaryliodonium(iii) salts have been used for the first time to realize a facile and clean one-pot synthesis of diaryliodonium(iii) salts 3 from aryl iodides 1 and suitable arene partners 2 with peracetic acid (PAA). The use of PAA as a green and practical oxidant is significantly effective in fluoroalcohol solvents. The scope and limitations of the methodology are elucidated by investigation of a wide variety of representative substrates.

An efficient one-pot synthesis of β-enamino ketones from endo glucal via hypervalent iodine

2010 ◽  
Vol 51 (46) ◽  
pp. 5996-5999 ◽  
Author(s):  
Zi-Ping Lin ◽  
Hsu-Hsuan Wu ◽  
Masayuki Kimura ◽  
Kimiyoshi Kaneko ◽  
Hiroyuki Takayama ◽  
...  
Keyword(s):  
Hypervalent Iodine ◽  
One Pot ◽  
Enamino Ketones ◽  
One Pot Synthesis

ChemInform Abstract: Solvent-Free One Pot Synthesis of 2-Aryl/Heteroarylbenzothiazoles Using Hypervalent Iodine(III) Reagents.

ChemInform ◽  
2013 ◽  
Vol 44 (16) ◽  
pp. no-no
Author(s):  
Parvin Kumar ◽  
Meenakshi Meenakshi ◽  
Sunil Kumar ◽  
Ashwani Kumar ◽  
Khalid Hussain ◽  
...  
Keyword(s):  
Solvent Free ◽  
Hypervalent Iodine ◽  
One Pot ◽  
One Pot Synthesis

ChemInform Abstract: One-Pot Synthesis of Hypervalent Iodine Reagents for Electrophilic Trifluoromethylation.

ChemInform ◽  
2013 ◽  
Vol 44 (49) ◽  
pp. no-no
Author(s):  
Vaclav Matsousek ◽  
Ewa Pietrasiak ◽  
Rino Schwenk ◽  
Antonio Togni
Keyword(s):  
Hypervalent Iodine ◽  
One Pot ◽  
One Pot Synthesis
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