Zobrazeno 1 - 10
of 32
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
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,
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.
Autor:
Dutta, Kamal K.1 (AUTHOR) chm2291001_kamal@cottonuniversity.ac.in, Sharma, Pranay1 (AUTHOR) pranay1234sharma@gmail.com, Banik, Subham1 (AUTHOR) chm2391001_subham@cottonuniversity.ac.in, Gomila, Rosa M.2 (AUTHOR) rosa.gomila@uib.es, Frontera, Antonio2 (AUTHOR) miquel.barcelo@uib.es, Barcelo-Oliver, Miquel2 (AUTHOR), Bhattacharyya, Manjit K.1 (AUTHOR) toni.frontera@uib.es
Publikováno v:
Inorganics. Oct2024, Vol. 12 Issue 10, p267. 21p.
Autor:
Barakat, Karim1 (AUTHOR), Ragheb, Mohamed A.1 (AUTHOR) mattia@cu.edu.eg, Soliman, Marwa H.1 (AUTHOR), Abdelmoniem, Amr M.2 (AUTHOR), Abdelhamid, Ismail A.2 (AUTHOR) ismail_shafy@cu.edu.eg
Publikováno v:
BMC Chemistry. 9/20/2024, Vol. 18 Issue 1, p1-17. 17p.
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
Autor:
Topală, Tamara Liana1 (AUTHOR) topala.liana@umfcluj.ro, Fizeşan, Ionel2 (AUTHOR) ionel.fizesan@umfcluj.ro, Petru, Andreea-Elena2 (AUTHOR) andreea.elen.petru@elearn.umfcluj.ro, Castiñeiras, Alfonso3 (AUTHOR) alfonso.castineiras@usc.es, Bodoki, Andreea Elena1 (AUTHOR) abota@umfcluj.ro, Oprean, Luminița Simona1 (AUTHOR) loprean@umfcluj.ro, Escolano, Marcos4 (AUTHOR) marcos.escolano@uv.es, Alzuet-Piña, Gloria5 (AUTHOR) gloria.alzuet@uv.es
Publikováno v:
Inorganics. Jun2024, Vol. 12 Issue 6, p158. 25p.
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
Autor:
KARTHICK, V.1 kv0994@srmist.edu.in, SUVITHA, V.1 suvithav@srmist.edu.in
Publikováno v:
Reliability: Theory & Applications. Dec2023, Vol. 18 Issue 4, p1019-1031. 13p.
Autor:
Karajgi, Santosh1, Gavit, Pankaj Ramesh2, Babasaheb, Jige Sandipan3, Rout, Dwity Sundar4, Chakrapani, Inavolu Srinivasa5, Bhattacharya, Sumanta6, Chinthamu, Narender7
Publikováno v:
Journal of Pharmaceutical Negative Results. 2023, Vol. 14 Issue 3, p696-703. 8p.