Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Cephalosporolide D"'
In this communication, a concise and efficient synthetic route for the synthesis of (–)-Cephalosporolide D in enantioselective way has been described. In this synthesis, Mitsunobu esterification and Ring Closing Metathesis (RCM) for macrocyclic rin
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https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15be97e9125e4170ea0d4f91074d48a
Akademický článek
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Autor:
Gurrala Alluraiah, Rudraraju Ramesh Raju, Palle Sadanandam, Reddymasu Sreenivasulu, Kowthalam Anitha
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 147:451-455
A concise stereoselective total synthesis of eight-membered lactone (−)-cephalosporolide D has been derived from inexpensive and commercially available starting material (S)-propylene epoxide. This concise synthesis utilizes Grignard reaction, Noyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8909e8b19b1d5cfa6d66f5fa781cb731
https://doi.org/10.1007/s00706-015-1526-4
https://doi.org/10.1007/s00706-015-1526-4
Autor:
Gurrala Alluraiah, Indraganti Sreenivasa Murthy, Rudraraju Ramesh Raju, Reddymasu Sreenivasulu
Publikováno v:
Letters in Organic Chemistry. 11:327-332
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::823cdb3828deb848e22b8e69277f3c74
https://doi.org/10.2174/1570178611666140124001937
https://doi.org/10.2174/1570178611666140124001937
Publikováno v:
European Journal of Chemistry. 5:127-132
A simple and efficient synthesis of eight-membered lactone, Cephalosporolide D has been accomplished from inexpensive and commercially available starting materials. This synthesis utilizes α-aminoxylation catalyzed by L-proline reaction, Jacobsen’
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13f645ceffcf7d3c8e59ccac090f2633
https://doi.org/10.5155/eurjchem.5.1.127-132.1002
https://doi.org/10.5155/eurjchem.5.1.127-132.1002
Autor:
J. Madhusudana Rao, R. Sateesh Chandra Kumar, Eppakayala Sreedhar, G. Venkateswar Reddy, K. Suresh Babu
Publikováno v:
Tetrahedron Letters. 51:1723-1726
A simple and efficient stereoselective synthesis of macrolactone, (+)-cephalosporolide D has been accomplished in 13 steps from inexpensive and commercially available starting materials in an overall yield of 17%, respectively. This convergent synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9426c4938e0e3a5702a500ed8fe89685
https://doi.org/10.1016/j.tetlet.2010.01.082
https://doi.org/10.1016/j.tetlet.2010.01.082
Publikováno v:
Bulletin of the Chemical Society of Japan. 84:229-231
The synthesis of an eight-membered lactone, cephalosporolide D is described using an iterative acetylene–epoxide coupling strategy. The terminal triple bond compound prepared in situ from the known...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::529b57e524f747ccf1cac7ff2a213476
https://doi.org/10.1246/bcsj.20100283
https://doi.org/10.1246/bcsj.20100283
Autor:
Indraganti Sreenivasa Murthy, Gurrala Alluraiah, Reddymasu Sreenivasulu, Rudraraju Ramesh Raju
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2f05386fd46af406c274b83dfdd7b04
https://doi.org/10.1002/chin.201443211
https://doi.org/10.1002/chin.201443211
Akademický článek
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Publikováno v:
ChemInform. 42
Title compound (VI) is synthesized using an iterative acetylene-epoxide coupling [ (III)] and a Yamaguchi lactonization as the key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36e4db74363d98fdb51cf75b5867873a
https://doi.org/10.1002/chin.201124192
https://doi.org/10.1002/chin.201124192