The SAMP-/RAMP-hydrazone methodology in asymmetric synthesis of 4S-ferrugineone and 4S,5S-ferrugineol: The pheromones of palm weevils

سال انتشار: 1393
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 684

فایل این مقاله در 10 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_ICC-2-2_006

تاریخ نمایه سازی: 18 تیر 1394

چکیده مقاله:

4S-ferrugineone and 4S,5S-ferrugineol as pheromones of palm weevils were synthesized in 3 and 4 steps, respectively, starting from nonane-5-one employing SAMP-/RAMP -hydrazone methodology. 5-Nonanone is transformed to its corresponding RAMP hydrazone by reaction with the enantiomerically pure hydrazine RAMP. Metalation with lithium diisopropylamide (LDA) in ether to form azaenolate, followed by methylation with methyl iodide, furnishes the product hydrazone. Finally, cleavage of the hydrazone moiety to regenerate the carbonyl functionality is possible by ozonolysis, leads to the 4S-ferrugineone. The crucial step would be the final diastereoselective reduction to the 4S, 5S-ferrugineol.

نویسندگان

Hamid Saeidian

Department of Science, Payame Noor University, P.O. Box ۱۹۳۹۵-۴۶۹۷, Tehran, Iran

Dieter Enders

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg ۱, ۵۲۰۷۴, Aachen, Germany

Zohreh Mirjafary

Department of Chemistry, Science and Research Branch Islamic Azad University, Tehran, Iran