NHC-Catalyzed Annulation of Enals to 2,4-Dien-1-ones: Efficient Diastereoselective Synthesis of 1,3-Diaryl-4-styrenyl Cyclopentenes
摘要:
Nucleophilic heterocyclic carbene (NHC)-catalyzed annulation strategy has been utilized for the efficient synthesis of styrenyl-substituted cyclopentenes from 2,4-dienones.
Synthesis, biological evaluation and QSAR studies of diarylpentanoid analogues as potential nitric oxideinhibitors
作者:S. M. Mohd Faudzi、S. W. Leong、F. Abas、M. F. F. Mohd Aluwi、K. Rullah、K. W. Lam、S. Ahmad、C. L. Tham、K. Shaari、N. H. Lajis
DOI:10.1039/c4md00541d
日期:——
A series of forty-five diarylpentadienone analogues were synthesized and were screened for their anti-inflammatory properties. Compound 7d had potent nitric oxide (NO) activity with an IC50 value of 10.24 μM.
NHC-Catalyzed Annulation of Enals to 2,4-Dien-1-ones: Efficient Diastereoselective Synthesis of 1,3-Diaryl-4-styrenyl Cyclopentenes
作者:V. Nair、C. Sinu、D. Padmaja、P. Jini、K. Lakshmi
DOI:10.1055/s-0033-1339308
日期:——
Nucleophilic heterocyclic carbene (NHC)-catalyzed annulation strategy has been utilized for the efficient synthesis of styrenyl-substituted cyclopentenes from 2,4-dienones.