Enantioselective total synthesis of cis-(+)- and trans-(+)-disparlure. Issue 34 (23rd August 2017)
- Record Type:
- Journal Article
- Title:
- Enantioselective total synthesis of cis-(+)- and trans-(+)-disparlure. Issue 34 (23rd August 2017)
- Main Title:
- Enantioselective total synthesis of cis-(+)- and trans-(+)-disparlure
- Authors:
- Garg, Yuvraj
Kumar Tiwari, Anand
Kumar Pandey, Satyendra - Abstract:
- Graphical abstract: Highlights: cis -(+)-Disparlure, a female gypsy moths sex pheromone. A concise and efficient asymmetric general approach for disparlure. Organocatalytic MacMillan's self aldol reaction and Wittig olefination key steps. Regioselective ring opening of an epoxide and Mitsunobu esterification reactions. Abstract: An expedient enantioselective synthetic approach for the gypsy moth sex-attractant pheromone cis -(+)-1 and trans -(+)-disparlure2 is described employing the optimized combination of organocatalytic MacMillan's self aldol reaction, Wittig olefination, regioselective ring opening of an epoxide and Mitsunobu esterification reactions as key steps.
- Is Part Of:
- Tetrahedron letters. Volume 58:Issue 34(2017)
- Journal:
- Tetrahedron letters
- Issue:
- Volume 58:Issue 34(2017)
- Issue Display:
- Volume 58, Issue 34 (2017)
- Year:
- 2017
- Volume:
- 58
- Issue:
- 34
- Issue Sort Value:
- 2017-0058-0034-0000
- Page Start:
- 3344
- Page End:
- 3346
- Publication Date:
- 2017-08-23
- Subjects:
- Sex-attractant pheromone -- Disparlure -- MacMillan's self aldol reaction -- Wittig olefination -- Mitsunobu esterification
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tetlet.2017.07.024 ↗
- Languages:
- English
- ISSNs:
- 0040-4039
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8796.860000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4672.xml