Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1254140 | Chinese Chemical Letters | 2014 | 5 Pages |
Abstract
Efficient and easily reproducible synthesis of sterically hindered multibrominated corroles is achieved via dipyrromethane-aldehyde condensation reaction in good yields. Boron trifluoride dietherate (BF3·Et2O) is found to be the effective catalyst for cyclization reaction, giving corrole as the major product.
Graphical abstractAn improved, facile method for the synthesis of sterically encumbered multibrominated corroles is described based on the use of boron trifluoride dietherate (BF3·Et2O) as the catalyst.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Mian HR Mahmood, Ze-Yu Liu, Hai-Yang Liu, Huai-Bo Zou, C.-K. Chang,