Asymmetric Strecker Reaction with Chiral Amines: a Catalyst-Free Protocol Using Acetone Cyanohydrin in Water

2013 ◽  
Vol 2013 (9) ◽  
pp. 1683-1695 ◽  
Author(s):  
Matteo Pori ◽  
Paola Galletti ◽  
Roberto Soldati ◽  
Daria Giacomini
Keyword(s):  
Chiral Amines ◽  
Acetone Cyanohydrin ◽  
Strecker Reaction ◽  
Catalyst Free

ChemInform Abstract: Asymmetric Strecker Reaction with Chiral Amines: A Catalyst-Free Protocol Using Acetone Cyanohydrin in Water.

ChemInform ◽  
2013 ◽  
Vol 44 (33) ◽  
pp. no-no
Author(s):  
Matteo Pori ◽  
Paola Galletti ◽  
Roberto Soldati ◽  
Daria Giacomini
Keyword(s):  
Chiral Amines ◽  
Acetone Cyanohydrin ◽  
Strecker Reaction ◽  
Catalyst Free

Catalyst-Free Multicomponent Strecker Reaction in Acetonitrile.

ChemInform ◽  
2006 ◽  
Vol 37 (12) ◽  
Author(s):  
Ricardo Martinez ◽  
Diego J. Ramon ◽  
Miguel Yus
Keyword(s):  
Strecker Reaction ◽  
Catalyst Free

Catalyst-free multicomponent Strecker reaction in acetonitrile

2005 ◽  
Vol 46 (49) ◽  
pp. 8471-8474 ◽  
Author(s):  
Ricardo Martínez ◽  
Diego J. Ramón ◽  
Miguel Yus
Keyword(s):  
Strecker Reaction ◽  
Catalyst Free

Synthesis of decahydropyrrolo[1,2-a]tetrazolo[1,5-d]pyrazines via Strecker reaction and intramolecular [3+2] cycloaddition

RSC Advances ◽  
2016 ◽  
Vol 6 (35) ◽  
pp. 29783-29793 ◽  
Author(s):  
Shakil N. Afraj ◽  
Chinpiao Chen ◽  
Gene-Hsian Lee
Keyword(s):  
Efficient Method ◽  
Strecker Reaction ◽  
Catalyst Free

An efficient method for synthesizing a series of novel (5aS,10R)-10-aryl-5,5a,6,7,8,10-hexahydropyrrolo[1,2-a]tetrazolo[1,5-d]pyrazines by using a catalyst-free three-component Strecker reaction followed by an intramolecular [3+2] cycloaddition.

ChemInform Abstract: Glycerol Mediated Strecker Reaction: Catalyst-Free Protocol for the Synthesis of α-Amino Nitriles.

ChemInform ◽  
2015 ◽  
Vol 46 (18) ◽  
pp. no-no
Author(s):  
Ramesh S. Ghogare ◽  
K. Rajeshwari ◽  
A. Venkat Narsaiah
Keyword(s):  
Strecker Reaction ◽  
Catalyst Free

An efficient and catalyst-free synthesis of N-arylidene-2-arylimidazo[1,2-a]pyridine-3-ylamine derivatives via Strecker reaction under controlled microwave heating

2017 ◽  
Vol 6 (4) ◽  
Author(s):  
Afaf Mohamed Abdel Hameed ◽  
Moustafa Sherief Moustafa ◽  
Saleh Mohammed Al-Mousawi ◽  
Reham R. Awed ◽  
Kamal Usef Sadek
Keyword(s):  
Microwave Heating ◽  
Multicomponent Reaction ◽  
Aromatic Aldehydes ◽  
Atom Economy ◽  
One Pot ◽  
Strecker Reaction ◽  
Catalyst Free ◽  
Benzoyl Cyanide

AbstractAn efficient one-pot multicomponent reaction of 2-aminopyridine with aromatic aldehydes and either benzoyl cyanide or cyanamide in pyridine under controlled microwave heating afforded N-aryldene-2-arylimidazo[1,2-a]-pyridine-3-ylamine derivatives. The reaction is catalyst free and is of high atom economy.

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