4.3 Article

Thiamine Hydrochloride-Catalyzed One-Pot Synthesis of 1,4-Dihydropyridine Derivatives Under Solvent-Free Conditions

Journal

SYNTHETIC COMMUNICATIONS
Volume 41, Issue 13, Pages 1969-1976

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00397911.2010.494814

Keywords

Aldehydes; 1; 4-dihydropyridines; Hantzsch reaction; -keto ester; thiamine hydrochloride (VB1)

Funding

  1. Chinese National Science and Technology [2009ZX09301-001, 2009ZX09102]
  2. Chinese National High-Tech RD Program [2007AA02Z147]
  3. National Natural Science Foundation of China [90713046, 30772638, 30925040]
  4. CAS Foundation [KSCX2-YW-R-179]

Ask authors/readers for more resources

[image omitted] An efficient one-pot synthesis of 1,4-dihydropyridines from an aldehyde, -keto ester, and ammonium acetate or formamidine acetate using thiamine hydrochloride (VB1) as the catalyst under solvent-free conditions at ambient temperature is described. All types of aldehydes, including aromatic, aliphatic, and unsaturated aldehydes, give good yields. The catalyst can easily be recovered after completion of the reaction and reused without affecting its activity.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available