Zobrazeno 1 - 10
of 15
pro vyhledávání: '"S. Rehana Anjum"'
Publikováno v:
Organic letters. 22(8)
Bioactive compounds featuring an unusual core of spiro[5.5]undecenes and calliviminones were synthesized in very good yield with good regio- and diastereoselectivities through a one-pot Knoevenagel and [4 + 2] cycloaddition from the readily available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c00e80cf547eb22985c6624925fac78f
https://pubmed.ncbi.nlm.nih.gov/32223251
https://pubmed.ncbi.nlm.nih.gov/32223251
Publikováno v:
RSC Advances. 6:75133-75137
A novel self-terminated Prins strategy has been developed for the synthesis of 2-substituted tetrahydropyran-4-one derivatives through a condensation of 3-(phenylthio)but-3-en-1-ol with carbonyl compounds in the presence of 5 mol% of Sc(OTf)3 under m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4dd28bf840c535acf992bb4553ffb8b9
https://doi.org/10.1039/c6ra11218h
https://doi.org/10.1039/c6ra11218h
Publikováno v:
European Journal of Organic Chemistry. 2014:4389-4397
A formal synthesis of herboxidiene/GEX 1A is described. This approach demonstrates successful application of the Prins cyclization for the construction of the tetrahydropyran core of the target molecule. The chirality of the side chain has been estab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6c903f9fd7519f44d5d97aaffbc3424
https://doi.org/10.1002/ejoc.201402235
https://doi.org/10.1002/ejoc.201402235
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4468ca4adceb83cd5ee7c3027fd4cd58
https://doi.org/10.1002/chin.201652277
https://doi.org/10.1002/chin.201652277
Publikováno v:
Tetrahedron Letters. 53:1790-1793
A tandem ene/Prins cyclization of olefin tethered aldehyde with an aldehyde has been accomplished using 5 mol % scandium triflate at ambient temperature to afford a novel series of cis-fused octahydropyrano[2,3-c]pyrrole derivatives in good yields wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be0e1fa66608324ac79965b6ddf8f1bc
https://doi.org/10.1016/j.tetlet.2012.01.117
https://doi.org/10.1016/j.tetlet.2012.01.117
Publikováno v:
Synlett. 2011:2951-2954
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94e8c6c74b0427ac26a13b645f919460
https://doi.org/10.1055/s-0031-1290084
https://doi.org/10.1055/s-0031-1290084
Publikováno v:
Tetrahedron Letters. 55:5011-5013
Various aldehydes undergo smooth coupling with 5-(hydroxymethyl)-4,6,6-trimethylcyclohex-3-enol in the presence of p-TSA at ambient temperature to afford a novel series of hexahydro-8,8-dimethyl-1H-isochromen-7-ol derivatives in good yields with high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6664ef4d1fbae854d6d0c24240c1caf8
https://doi.org/10.1016/j.tetlet.2014.07.072
https://doi.org/10.1016/j.tetlet.2014.07.072
Publikováno v:
ChemInform. 46
A formal synthesis of herboxidiene/GEX 1A is described. This approach demonstrates successful application of the Prins cyclization for the construction of the tetrahydropyran core of the target molecule. The chirality of the side chain has been estab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10e639d15cd880068fdee126e07a6104
https://doi.org/10.1002/chin.201509283
https://doi.org/10.1002/chin.201509283
Publikováno v:
ChemInform. 46
Various aldehydes undergo smooth coupling with 5-(hydroxymethyl)-4,6,6-trimethylcyclohex-3-enol in the presence of p-TSA at ambient temperature to afford a novel series of hexahydro-8,8-dimethyl-1H-isochromen-7-ol derivatives in good yields with high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73127ad3fcdc10f31714fc2762fc1339
https://doi.org/10.1002/chin.201508212
https://doi.org/10.1002/chin.201508212
Publikováno v:
Tetrahedron Letters. 50:6029-6031
Aldehyde, alcohol, azide, and alkyne undergo smooth coupling by means of acetal formation, azidation, and a subsequent ‘click reaction’ in the presence of copper(II) triflate and copper metal in acetonitrile to furnish α-alkoxy-1,2,3-triazoles i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42f3cbceb18143d1924dd2716e425793
https://doi.org/10.1016/j.tetlet.2009.08.027
https://doi.org/10.1016/j.tetlet.2009.08.027