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Information Journal Paper

Title

PREPARATION OF 3,4-DIPHENYL-4- METHOXY- 2- CYCLOPENTENE-L-OL AND ITS DERIVATIVES

Pages

  229-234

Keywords

Not Registered.

Abstract

 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.

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  • Cite

    APA: Copy

    MARJANI, K., SHARIFI MOGHADAM KAKHAKI, M., & MOSAVI, M.. (2003). PREPARATION OF 3,4-DIPHENYL-4- METHOXY- 2- CYCLOPENTENE-L-OL AND ITS DERIVATIVES. JOURNAL OF SCIENCE (KHARAZMI UNIVERSITY), 3(1-2), 229-234. SID. https://sid.ir/paper/357695/en

    Vancouver: Copy

    MARJANI K., SHARIFI MOGHADAM KAKHAKI M., MOSAVI M.. PREPARATION OF 3,4-DIPHENYL-4- METHOXY- 2- CYCLOPENTENE-L-OL AND ITS DERIVATIVES. JOURNAL OF SCIENCE (KHARAZMI UNIVERSITY)[Internet]. 2003;3(1-2):229-234. Available from: https://sid.ir/paper/357695/en

    IEEE: Copy

    K. MARJANI, M. SHARIFI MOGHADAM KAKHAKI, and M. MOSAVI, “PREPARATION OF 3,4-DIPHENYL-4- METHOXY- 2- CYCLOPENTENE-L-OL AND ITS DERIVATIVES,” JOURNAL OF SCIENCE (KHARAZMI UNIVERSITY), vol. 3, no. 1-2, pp. 229–234, 2003, [Online]. Available: https://sid.ir/paper/357695/en

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