Zobrazeno 1 - 10 of 1 163 pro vyhledávání: '"Jhillu S. Yadav"'
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Akademický článek
Stereoselective synthesis of four possible isomers of streptopyrrolidine
Autor: Debendra K. Mohapatra, Barla Thirupathi, Pragna P. Das, Jhillu S. Yadav
Publikováno v: Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 34-39 (2011)
The synthesis of (4R,5R)-streptopyrrolidine (1), (4S,5R)-streptopyrrolidine (2) (4R,5S)-streptopyrrolidine (3) and (4S,5S)-streptopyrrolidine (4) have been achieved in a concise and highly efficient manner via a highly stereoselective aldol type reac
Externí odkaz: https://doaj.org/article/96ea39a2301b4624b905df78e794887a
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3
Akademický článek
Synthesis of (3R,5R)-harzialactone A and its (3R,5S)-isomer
Autor: Gowravaram Sabitha, Rangavajjula Srinivas, Sukant K. Das, Jhillu S. Yadav
Publikováno v: Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, p 8 (2010)
The total synthesis of (3R,5R)-harzialactone A (1) and its (3R,5S)-isomer (2) is described. Epoxide opening with thioacetal and diastereoselective reductions are used as key reactions.
Externí odkaz: https://doaj.org/article/0cbf944477374a3c9df4cd25bf81ba00
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6
Total Synthesis and Structural Revision of Greensporone F and Dechlorogreensporone F
Autor: Jhillu S. Yadav, Aedula Vishnu V. Reddy, A. V. S. Sarma, Janardhan Gaddam, Debendra K. Mohapatra
Publikováno v: The Journal of Organic Chemistry. 85:12418-12429
The first asymmetric total syntheses of the real isolation product (2S,5R,8R)-greensporone F and (2S,5R,8R)-dechlorogreensporone F, 14-membered resorcylic acid lactones with a cis-2,5-disubstituted...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b34f6e5e9991c4d7f873a16ea4e0b16
https://doi.org/10.1021/acs.joc.0c01644
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9
Synthesis of chiral propargyl alcohols following the base-induced elimination protocol: application in the total synthesis of natural products
Autor: Jhillu S. Yadav, Uma Maheshwar Gonela
Publikováno v: New Journal of Chemistry. 44:4972-4986
Synthesis of enantiomerically pure propargyl alcohols is one of the most important tools in organic synthesis. Base-induced elimination of β-alkoxy chlorides could offer enantiomerically pure propargyl alcohols corresponding to their precursor. This
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8675011bb427941e80892fcd33a8f17f
https://doi.org/10.1039/c9nj05626b
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Metal free montmorillonite KSF clay catalyzed practical synthesis of benzoxazoles and benzothiazoles under aerobic conditions
Autor: Vijaya Babu Kummari, Rathod Aravind Kumar, Kalavakuntla Chiranjeevi, Alleni Suman Kumar, Jhillu S. Yadav
Publikováno v: Synthetic Communications. 49:3335-3342
An efficient method for the synthesis of benzoxazoles and benzothiazoles via montmorillonite KSF clay catalyzed condensation reaction between 2-aminophenols or 2-aminothiophenols and β-diketones is reported. The efficiency of the reaction reflects f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3df9a4584c5f4e3ef13ba040cd472c89
https://doi.org/10.1080/00397911.2019.1665183
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