Chiral Primary−Tertiary Diamine−Brønsted Acid Salt Catalyzed Syn-Selective Cross-Aldol Reaction of Aldehydes

2010 ◽  
Vol 75 (13) ◽  
pp. 4501-4507 ◽  
Author(s):  
Jiuyuan Li ◽  
Niankai Fu ◽  
Xin Li ◽  
Sanzhong Luo ◽  
Jin-Pei Cheng
Keyword(s):  
Aldol Reaction ◽  
Bronsted Acid ◽  
Acid Salt ◽  
Brønsted Acid ◽  
Brönsted Acid

scholarly journals Brønsted Acid Catalyzed Asymmetric Aldol Reaction: A Complementary Approach to Enamine Catalysis

2010 ◽  
Vol 12 (16) ◽  
pp. 3582-3585 ◽  
Author(s):  
Guillaume Pousse ◽  
Fabien Le Cavelier ◽  
Luke Humphreys ◽  
Jacques Rouden ◽  
Jérôme Blanchet
Keyword(s):  
Aldol Reaction ◽  
Bronsted Acid ◽  
Brønsted Acid ◽  
Asymmetric Aldol ◽  
Complementary Approach ◽  
Brönsted Acid ◽  
Asymmetric Aldol Reaction ◽  
Enamine Catalysis ◽  
Acid Catalyzed

Catalyst-free synthesis of α1-oxindole-α-hydroxyphosphonates via phospha-aldol reaction of isatins employing N-heterocyclic phosphine (NHP)-thiourea

2016 ◽  
Vol 14 (38) ◽  
pp. 8952-8956 ◽  
Author(s):  
Nagaraju Molleti ◽  
Jun Yong Kang
Keyword(s):  
Critical Role ◽  
Aldol Reaction ◽  
Bronsted Acid ◽  
Brønsted Acid ◽  
Catalyst Free ◽  
Brönsted Acid

A catalyst-free phospha-aldol reaction of isatins with NHP-thiourea has been developed and the critical role of the Brønsted acid in this transformation is unveiled.

A phosphotungstic acid-supported multifunctional organocatalyst containing 9-amino(9-deoxy)epi-cinchonidine and Brønsted acid and its application in asymmetric aldol reaction

RSC Advances ◽  
2016 ◽  
Vol 6 (61) ◽  
pp. 55894-55902 ◽  
Author(s):  
Ling Lan ◽  
Guangxin Xie ◽  
Tao Wu ◽  
Dandan Feng ◽  
Xuebing Ma
Keyword(s):  
Phosphotungstic Acid ◽  
Aldol Reaction ◽  
Catalytic Performance ◽  
Bronsted Acid ◽  
Brønsted Acid ◽  
Asymmetric Aldol ◽  
Brönsted Acid ◽  
Asymmetric Aldol Reaction ◽  
First Time ◽  
Excellent Catalytic Performance

Phosphotungstic acid-supported multifunctional 9-amino(9-deoxy)epi-cinchonidine containing Brønsted acid was developed through facile precipitation for the first time and afforded aldol adducts in excellent catalytic performance with good reusability.

An environmentally friendly Mukaiyama aldol reaction catalyzed by a strong Brønsted acid in solvent-free conditions

2011 ◽  
Vol 9 (7) ◽  
pp. 2192 ◽  
Author(s):  
Margherita Barbero ◽  
Stefano Bazzi ◽  
Silvano Cadamuro ◽  
Stefano Dughera ◽  
Claudio Magistris ◽  
...  
Keyword(s):  
Aldol Reaction ◽  
Environmentally Friendly ◽  
Solvent Free ◽  
Bronsted Acid ◽  
Brønsted Acid ◽  
Mukaiyama Aldol Reaction ◽  
Solvent Free Conditions ◽  
Brönsted Acid ◽  
Mukaiyama Aldol

Brønsted acid mediated N–O bond cleavage for α-amination of ketones through the aromatic nitroso aldol reaction

2016 ◽  
Vol 52 (15) ◽  
pp. 3215-3218 ◽  
Author(s):  
Isai Ramakrishna ◽  
Harekrishna Sahoo ◽  
Mahiuddin Baidya
Keyword(s):  
Bond Cleavage ◽  
Aldol Reaction ◽  
Nitroso Compounds ◽  
Bronsted Acid ◽  
Brønsted Acid ◽  
Enol Ethers ◽  
Silyl Enol Ethers ◽  
Brönsted Acid ◽  
Aromatic Nitroso Compounds

A Brønsted acid mediated N–O bond cleavage for α-amination of ketones has been developed through the nitroso aldol reaction of less-reactive aromatic nitroso compounds and silyl enol ethers having a disilane (–SiMe2TMS) backbone.

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