Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/8966| Title: | Synthesis of 2,3-trans-3,4-trans-2-aryl-3-alkyl/aryl chroman-4-ols |
| Authors: | Venkati, M Krupadanam, G L David |
| Issue Date: | Mar-2005 |
| Publisher: | CSIR |
| IPC Code: | Int.Cl.7 C 07 D 311/30 |
| Abstract: | -Alkyl
chalcones 3a-d on acid catalyzed
cyclization give a mixture of (±) trans and (±) cis 2-aryl-3-alkylchroman-4-ones.
cis 4a-d are converted to trans
5a-d by epimerization with dil.
alkali. a-Aryl chalcones 3e-h on acid catalyzed cyclization give (±) trans
2,3-diaryl-chroman-4-ones 5e-h. On
NaBH4 reduction 5a-h give
(±) 2,3-trans-3,4-trans-2-aryl-3-alkyl/aryl- chroman-4-ols
6a-h. |
| Page(s): | 618-621 |
| ISSN: | 0975-0983(Online); 0376-4699(Print) |
| Appears in Collections: | IJC-B Vol.44B(03) [March 2005] |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 44B(3) 618-621.pdf | 109.3 kB | Adobe PDF | View/Open |
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-Alkyl
chalcones 3a-d on acid catalyzed
cyclization give a mixture of (±) trans and (±) cis 2-aryl-3-alkylchroman-4-ones.
cis 4a-d are converted to trans
5a-d by epimerization with dil.
alkali. a-Aryl chalcones 3e-h on acid catalyzed cyclization give (±) trans
2,3-diaryl-chroman-4-ones 5e-h. On
NaBH4 reduction 5a-h give
(±) 2,3-trans-3,4-trans-2-aryl-3-alkyl/aryl- chroman-4-ols
6a-h.