Lewis acid promoted synthesis of methylene-bridged α-and γ-bis-benzopyrones
NOPR - NISCAIR Online Periodicals Repository
View Archive InfoField | Value | |
Title |
Lewis acid promoted synthesis of methylene-bridged α-and γ-bis-benzopyrones
|
|
Creator |
Kumar, Sandeep
Prasad, Ashok K Mehta, Shilpika Bali |
|
Subject |
O-Methoxyacetyl derivatives of hydroxyl-chromanones
coumarins and chromones Lewis acid methylenebridged bis-benzopyrones Fries rearrangement |
|
Description |
43-50
The Lewis acid promoted Fries rearrangement of O-methoxyacetyl derivatives of hydroxy-chromanones, coumarins and chromones under solvent-free condition gives isomeric methylene-bridged bischromanones, biscoumarins and bischromones, respectively, in good yields. The benzopyrone precursors undergo intermolecular rearrangement wherein two benzopyrone moieties are joined through their benzene rings via an un-substituted methylene bridge. |
|
Date |
2022-02-01T11:42:12Z
2022-02-01T11:42:12Z 2022-01 |
|
Type |
Article
|
|
Identifier |
2583-1321 (Online); 0019-5103 (Print)
http://nopr.niscair.res.in/handle/123456789/59040 |
|
Language |
en
|
|
Publisher |
NIScPR-CSIR, India
|
|
Source |
IJC Vol.61(01) [January 2022]
|
|