Volume 18, Issue 57 (No.1&2-صفحات انگلیسی از 74 تا 82 2004)
2004, 18(57): 229-236 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Preparation of 3,4-diphenyl-4- methoxy-2- cyclopentene-1-ol and its derivatives. Journal title 2004; 18 (57) :229-236
URL: http://jsci.khu.ac.ir/article-1-1147-en.html
URL: http://jsci.khu.ac.ir/article-1-1147-en.html
Abstract: (3794 Views)
Reduction of methoxyketon 1 by NaBH4 gives methoxyketol 2. Allthough acetate and tosylate of this alchohol were not seprated, benzoate ester was isolated. Reduction of ketol 2 by LiAlH4 gives alchohol 4. Ketol 9 does not react with methyl magnesium iodide, but methoxyketon 1 react with both methyl magnesium iodide and phenyl magnesium iodide gives corresponding hydrocarbons. Keton 13 with phenylmagnesium iodide transforms to hydrocarbon 14. Compound 12 and 14 are light sensitive, disposing to light will change each of them to a mixture.
Keywords: Keton 13 with phenylmagnesium iodide
Published: 2004/01/15
| Rights and permissions | |
 | This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
