A facile synthesis of (+/-)-mintlactone

Date

1997-01-01

Author

Tanyeli, Cihangir
Demir, AS

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(+/-)-Mintlactone has been synthesized by applying a novel effective synthetic sequence. 4-Methylcyclohexanone was subjected to acetoxylation with Pb(OAc)(4). Hydrolysis followed by reaction with 2-chloroprogionyl chloride,then treatment with triethyl phosphite and, finally, Horner-Emmons-type intramolecular cyclization afforded (+/-)-Mintlactone.

Subject Keywords

Organic Chemistry

URI

https://hdl.handle.net/11511/45832

Journal

SYNTHETIC COMMUNICATIONS

DOI

https://doi.org/10.1080/00397919708005649

Collections

Department of Chemistry, Article

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Citation Formats

C. Tanyeli and A. Demir, “A facile synthesis of (+/-)-mintlactone,” SYNTHETIC COMMUNICATIONS, pp. 3471–3476, 1997, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/45832.