Zobrazeno 1 - 7
of 7
pro vyhledávání: '"K. Anantha Lakshmi"'
Autor:
Jhillu S. Yadav, K. Anantha Lakshmi, A. Ramachandra Prasad, N. Swapnil, N. Mallikarjuna Reddy
Publikováno v:
Tetrahedron: Asymmetry. 23:1155-1160
The stereoselective total synthesis of decarestrictine O, a polyketide natural product is described. The synthesis involves MacMillan α-hydroxylation, C1-Wittig olefination, hydrolytic kinetic resolution and ring closing metathesis (RCM) as key step
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd8c47703990f7e3a26ab1d210f9185d
https://doi.org/10.1016/j.tetasy.2012.06.027
https://doi.org/10.1016/j.tetasy.2012.06.027
Autor:
Ahmad Al Khazim Al Ghamdi, Attaluri R. Prasad, N. Mallikarjuna Reddy, Jhillu S. Yadav, K. Anantha Lakshmi
Publikováno v:
Synthesis. 44:2595-2600
A convergent approach to the total synthesis of (–)-invictolide, a component of the queen recognition pheromone of Solenopsis invicta, is described. Key steps involve the desymmetrization of a bicyclic olefin with Brown’s chiral hydroboration,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29d7bba1c33b45459707c7160e12ae05
https://doi.org/10.1055/s-0032-1316561
https://doi.org/10.1055/s-0032-1316561
Autor:
Jhillu S. Yadav, Basi V. Subba Reddy, K. Anantha Lakshmi, N. Mallikarjuna Reddy, Attaluri R. Prasad
Publikováno v:
Tetrahedron. 66:334-338
Stereoselective total synthesis of decarestrictine-J, a polyketide natural product is described. The synthesis involves the Prins cyclisation and Ring Closing Metathesis (RCM) as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cce8dcbebaf68453daa359d41a431d7a
https://doi.org/10.1016/j.tet.2009.10.100
https://doi.org/10.1016/j.tet.2009.10.100
Publikováno v:
Tetrahedron Letters. 51:661-663
The silylated secondary homopropargylic alcohols undergo smooth coupling with aldehydes in the presence of molecular iodine under mild reaction conditions to produce 4-iododihydropyrans in good yields. This method is highly stereoselective, affording
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7950bf23b521168a2b79c5ecbc614a57
https://doi.org/10.1016/j.tetlet.2009.11.103
https://doi.org/10.1016/j.tetlet.2009.11.103
Publikováno v:
ChemInform. 41
The silylated secondary homopropargylic alcohols undergo smooth coupling with aldehydes in the presence of molecular iodine under mild reaction conditions to produce 4-iododihydropyrans in good yields. This method is highly stereoselective, affording
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68b9d268ee27373ec63f3993b455aac0
https://doi.org/10.1002/chin.201019123
https://doi.org/10.1002/chin.201019123
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Akademický článek
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