Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pendyala Venkata Arun Kumar"'
Publikováno v:
Helvetica Chimica Acta. 98:1115-1126
Total syntheses of iso-cladospolide B (1) and the 12-membered macrolactone (6S,12R)-6-hydroxy-12-methyloxacyclododecane-2,5-dione (2), a non-natural product, were achieved from a common intermediate starting from commercially available 1,9-nonane dio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ae0134b2c7df4f361b986aa6b54d6f1
https://doi.org/10.1002/hlca.201500030
https://doi.org/10.1002/hlca.201500030
Autor:
Kallaganti V. S. Ramakrishna, Pendyala Venkata Arun Kumar, Venkata Satyanarayana Mallula, Palakodety Radha Krishna
Publikováno v:
Tetrahedron. 69:2319-2326
Stereoselective total synthesis of isomers of [2-phenyl-propionyl]-2-piperidinone-3( R )-yl-ester has been achieved using commercially available starting materials like trans cinnamaldehyde and 4-pentene-1-ol. The key steps are Steglich conditions fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2ac1420e57829761b04d36bfdb3a695
https://doi.org/10.1016/j.tet.2013.01.014
https://doi.org/10.1016/j.tet.2013.01.014
Publikováno v:
Helvetica Chimica Acta. 95:1623-1629
A new polyketide metabolite, the twelve-membered macrolide 1, isolated from the endophytic fungal strain Cladosporium tenuissimum LR 463 of Maytenus hookeri, whose structure had been determined as (6R,12S)-6-hydroxy-12-methyl-1-oxacyclododecane-2,5-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bad42c15fe858b7365c075795b1e01d5
https://doi.org/10.1002/hlca.201200064
https://doi.org/10.1002/hlca.201200064
Publikováno v:
Tetrahedron Letters. 53:4997-4999
The first total synthesis of helicascolides A and C is reported via acid catalyzed acetonide deprotection followed by intramolecular lactonization in one-pot as the key step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87368f12022b32592aea46ee97ffaee8
https://doi.org/10.1016/j.tetlet.2012.07.018
https://doi.org/10.1016/j.tetlet.2012.07.018