Stereoselective synthesis of (−)-tetrahydropyrenophorol

Autor:	Reddymasu Sreenivasulu, Bommareddy Pratapareddy, Vuppula Naresh Kumar, Mandava Venkata Basaveswara Rao, Rudraraju Ramesh Raju, Pradeepkumar Thota, Islavathu Hatti
Rok vydání:	2016
Předmět:	010405 organic chemistry Chemistry Epoxide Regioselectivity General Chemistry 010402 general chemistry Ring (chemistry) Photochemistry 01 natural sciences Combinatorial chemistry 0104 chemical sciences chemistry.chemical_compound Dihydroxylation Mitsunobu reaction Stereoselectivity
Zdroj:	Monatshefte für Chemie - Chemical Monthly. 148:751-756
ISSN:	1434-4475 0026-9247
DOI:	10.1007/s00706-016-1754-2
Popis:	A simple and efficient synthesis of macrocyclic dilactone tetrahydropyrenophorol has been accomplished from inexpensive and commercially available starting materials. This concise synthesis utilizes regioselective ring opening of epoxide, asymmetric dihydroxylation, and Mitsunobu reaction for the construction of the macrolactone.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::e133d1ba41740933f51d1bbf9813705c https://doi.org/10.1007/s00706-016-1754-2 Zobrazit plný text záznamu Full text from SpringerLink