Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Bommareddy Pratapareddy"'
Autor:
Reddymasu Sreenivasulu, Bommareddy Pratapareddy, Vuppula Naresh Kumar, Mandava Venkata Basaveswara Rao, Rudraraju Ramesh Raju, Pradeepkumar Thota, Islavathu Hatti
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 148:751-756
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e133d1ba41740933f51d1bbf9813705c
https://doi.org/10.1007/s00706-016-1754-2
https://doi.org/10.1007/s00706-016-1754-2
Autor:
Bommareddy Pratapareddy, Reddymasu Sreenivasulu, Mandava Venkata Basaveswara Rao, Rudraraju Ramesh Raju
Stereoselective total synthesis of Patulolide C has been accomplished from easily available and inexpensive (S)-chiral epoxide. The key steps involved in the concise synthesis of Patulolide C utilizes ring opening of chiral epoxide, cleavage of 1,2-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e1e58e197bf0015c46bface5edbdc86
Autor:
Bommareddy Pratapareddy, Reddymasu Sreenivasulu, Mandava Venkata Basaveswara Rao, Rudraraju Ramesh Raju
Stereoselective total synthesis of Patulolide C has been accomplished from easily available and inexpensive (S)-chiral epoxide. The key steps involved in the concise synthesis of Patulolide C utilizes ring opening of chiral epoxide, cleavage of 1,2-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::221d1418a50e2d0427e18d1298d982c0
Autor:
Bommareddy Pratapareddy, Rudraraju Ramesh Raju, Mandava Venkata Basaveswara Rao, Islavathu Hatti, Reddymasu Sreenivasulu
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 146:1921-1926
An asymmetric total synthesis of diplodialide C has been achieved starting from commercially available homoallylic alcohol. Regioselective opening of the chiral epoxide, cross-metathesis reaction, and Yamaguchi macrolactonization were used as the key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::059eeeb080dbb123eb0368c08c1c787b
https://doi.org/10.1007/s00706-015-1464-1
https://doi.org/10.1007/s00706-015-1464-1