Microwave-Assisted K-10 Montmorillonite Clay–Mediated Knoevenagel Hetero-Diels–Alder Reactions: A Novel Protocol for the Synthesis of Polycyclic Pyrano[2,3,4-kl]xanthene Derivatives
摘要:
The intramolecular hetero-Diels-Alder reactions of 2-(cyclohex-2-enyloxy)benzaldehyde by Knoevenagel condensation with symmetrical 1,3-diones under three different conditions afforded the pyrano[2,3,4-kl]xanthene derivatives in a stereoselective manner in good yield. The structure of one of the products was unambiguously established by x-ray analysis.
Microwave-Assisted K-10 Montmorillonite Clay–Mediated Knoevenagel Hetero-Diels–Alder Reactions: A Novel Protocol for the Synthesis of Polycyclic Pyrano[2,3,4-kl]xanthene Derivatives
摘要:
The intramolecular hetero-Diels-Alder reactions of 2-(cyclohex-2-enyloxy)benzaldehyde by Knoevenagel condensation with symmetrical 1,3-diones under three different conditions afforded the pyrano[2,3,4-kl]xanthene derivatives in a stereoselective manner in good yield. The structure of one of the products was unambiguously established by x-ray analysis.
Microwave-Assisted K-10 Montmorillonite Clay–Mediated Knoevenagel Hetero-Diels–Alder Reactions: A Novel Protocol for the Synthesis of Polycyclic Pyrano[2,3,4-<i>kl</i>]xanthene Derivatives
作者:Ekambaram Ramesh、Raghavachary Raghunathan
DOI:10.1080/00397910802417825
日期:2009.1.28
The intramolecular hetero-Diels-Alder reactions of 2-(cyclohex-2-enyloxy)benzaldehyde by Knoevenagel condensation with symmetrical 1,3-diones under three different conditions afforded the pyrano[2,3,4-kl]xanthene derivatives in a stereoselective manner in good yield. The structure of one of the products was unambiguously established by x-ray analysis.