Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shivashankar Kattela"'
Autor:
Shivashankar Kattela, Carlos Roque D. Correia, Abel Ros, Valentín Hornillos, Javier Iglesias-Sigüenza, Rosario Fernández, José M. Lassaletta
Publikováno v:
Organic Letters. 24:3812-3816
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f108dac9907bde0a54cc4d1c9c8ed958
https://doi.org/10.1021/acs.orglett.2c01355
https://doi.org/10.1021/acs.orglett.2c01355
Publikováno v:
Advanced Synthesis & Catalysis. 359:260-267
Enantioselective carbonyl-directable Heck reactions using aryldiazonium salts were developed with the aim to construct chiral quaternary spiro centers in an efficient manner. Five- and six-membered spirooxindoles, spirolactones, and spirolactams (36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bb0a09cb51f23cc0d40d2cb6e21f735
https://doi.org/10.1002/adsc.201600946
https://doi.org/10.1002/adsc.201600946
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(67)
In this communication, the enantioselective synthesis of phthalides and isochromanones is described through a new palladium-catalyzed Heck-Matsuda arylation/NaBH4 -reduction/lactonization sequence of 2,3- and 2,5-dihydrofurans in good overall yields
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d4c8d3158545c2978433b5bfafec235
https://pubmed.ncbi.nlm.nih.gov/30290051
https://pubmed.ncbi.nlm.nih.gov/30290051
Publikováno v:
Organicbiomolecular chemistry. 14(40)
A novel, efficient and enantioselective Heck-Matsuda desymmetrization of non-activated cyclopentene-fused spiro-pyrrolidinones was developed. The reaction provided the Heck products in good to excellent yields and selectivities and tolerated a variet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e27c932768286de76d0fda47b1808df
https://pubmed.ncbi.nlm.nih.gov/27722726
https://pubmed.ncbi.nlm.nih.gov/27722726