Aldol condensation reactions of acetone and formaldehyde over vanadium phosphate catalysts: Comments on the acid–base properties

2002 ◽  
Vol 4 (4) ◽  
pp. 688-695 ◽  
Author(s):  
Richard Tanner ◽  
Philip Gill ◽  
Richard Wells ◽  
Jillian E. Bailie ◽  
Gordon Kelly ◽  
...  
Keyword(s):  
Aldol Condensation ◽  
Vanadium Phosphate ◽  
Acid Base ◽  
Condensation Reactions ◽  
Aldol Condensation Reactions ◽  
Base Properties

Aldol condensation reactions of acetone over alkali-modified vanadium phosphate catalysts

2002 ◽  
Vol 4 (18) ◽  
pp. 4555-4560 ◽  
Author(s):  
Lee Thomas ◽  
Richard Tanner ◽  
Philip Gill ◽  
Richard Wells ◽  
Jillian E. Bailie ◽  
...  
Keyword(s):  
Aldol Condensation ◽  
Vanadium Phosphate ◽  
Condensation Reactions ◽  
Aldol Condensation Reactions

ChemInform Abstract: A Diphenylprolinol TMS Ether/Bile Acid Organocatalytic System for the Asymmetric Domino Sulfa-Michael/Aldol Condensation Reactions of 1,4-Dithiane-2,5-diol and Cinnamaldehydes.

ChemInform ◽  
2010 ◽  
Vol 41 (24) ◽  
pp. no-no
Author(s):  
Nikla Baricordi ◽  
Simonetta Benetti ◽  
Carmela De Risi ◽  
Marco Fogagnolo ◽  
Gian Piero Pollini ◽  
...  
Keyword(s):  
Bile Acid ◽  
Aldol Condensation ◽  
Condensation Reactions ◽  
Aldol Condensation Reactions

Unusual Domino Michael/Aldol Condensation Reactions Employing Oximes as N-Selective Nucleophiles: Synthesis ofN-Hydroxypyrroles

2009 ◽  
Vol 121 (4) ◽  
pp. 772-775 ◽  
Author(s):  
Bin Tan ◽  
Zugui Shi ◽  
Pei Juan Chua ◽  
Yongxin Li ◽  
Guofu Zhong
Keyword(s):  
Aldol Condensation ◽  
Condensation Reactions ◽  
Aldol Condensation Reactions

Supported Choline Hydroxide (Ionic Liquid) as Heterogeneous Catalyst for Aldol Condensation Reactions.

ChemInform ◽  
2004 ◽  
Vol 35 (36) ◽  
Author(s):  
Sonia Abello ◽  
Francisco Medina ◽  
Xavier Rodriguez ◽  
Yolanda Cesteros ◽  
Pilar Salagre ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Heterogeneous Catalyst ◽  
Aldol Condensation ◽  
Condensation Reactions ◽  
Aldol Condensation Reactions

scholarly journals Development of pharmaceutically relevant bio-based intermediates though aldol condensation and Claisen–Schmidt reactions of dihydrolevoglucosenone (Cyrene®)

2018 ◽  
Vol 20 (19) ◽  
pp. 4423-4427 ◽  
Author(s):  
Liam Hughes ◽  
Con R. McElroy ◽  
Adrian C. Whitwood ◽  
Andrew J. Hunt
Keyword(s):  
Aldol Condensation ◽  
Condensation Reactions ◽  
Aldol Condensation Reactions

Dihydrolevoglucosenone (Cyrene®) has been successfully utilised as a bio-based platform molecule for the synthesis of pharmaceutically relevant intermediates through aldol condensation reactions.

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