Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sudip Shit"'
Publikováno v:
The Journal of Organic Chemistry. 88:3012-3021
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5bd13b7d4e7545fbe5ffac3bd188aa7
https://doi.org/10.1021/acs.joc.2c02715
https://doi.org/10.1021/acs.joc.2c02715
Publikováno v:
The Journal of Organic Chemistry. 87:9259-9269
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6543e43b6b95fcfc25aa8a603695a5b1
https://doi.org/10.1021/acs.joc.2c00991
https://doi.org/10.1021/acs.joc.2c00991
Publikováno v:
The Journal of organic chemistry. 87(14)
An efficient methodology has been developed for the synthesis of both di- and trisubstituted thiazol-2(3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06af0a7311a3f1e592d984dcc3de6dcd
https://pubmed.ncbi.nlm.nih.gov/35772023
https://pubmed.ncbi.nlm.nih.gov/35772023
Publikováno v:
Synthesis. 52:1425-1434
An intramolecular Friedel–Crafts cyclization reaction catalyzed by indium(III) chloride for the formation of 4-vinyl-1,2,3,4-tetrahydroisoquinoline from N-tethered benzyl-alkenol in good yields has been described. The reaction is highly regioselect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6c49189e5f2ec4732fa4f49a54515a5
https://doi.org/10.1055/s-0037-1610750
https://doi.org/10.1055/s-0037-1610750
Publikováno v:
The Journal of Organic Chemistry. 85:1961-1971
A one-pot tandem reaction has been developed for the synthesis of substituted tetrahydropyrroloisoindolone via Mannich reaction of N-propargyl amido alcohols with 1,3-dicarbonyl compounds followed by Conia-ene cyclization reaction in moderate to good
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f93a64d0aa0ce11706ee35cbf00641b2
https://doi.org/10.1021/acs.joc.9b02686
https://doi.org/10.1021/acs.joc.9b02686
Publikováno v:
The Journal of organic chemistry. 85(4)
A one-pot tandem reaction has been developed for the synthesis of substituted tetrahydropyrroloisoindolone via Mannich reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::32efe15ba512e22c251e6b0a47c676fb
https://pubmed.ncbi.nlm.nih.gov/31912735
https://pubmed.ncbi.nlm.nih.gov/31912735
Publikováno v:
Organicbiomolecular chemistry. 17(31)
A novel synthetic route for the cyclization of ((4S,5R)-2,2-dimethyl-5-vinyl-1,3-dioxolan-4-yl)methanol with aldehydes to give hexahydrofuro[3,4-b]furan-4-ol and its dimer was developed. A variety of substituted furanol (up to 86%) and its bis-deriva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16e320fc87507424a6de117af36cd89c
https://pubmed.ncbi.nlm.nih.gov/31347626
https://pubmed.ncbi.nlm.nih.gov/31347626