Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Praveen AnkiReddy"'
Publikováno v:
ChemistrySelect. 2:1032-1036
Synthesis of a silyl derivative of revised aglycone of marine anticancer macrolide Mandelalide A is described. The synthetic highlights include acid catalyzed epoxide opening, Chelation- controlled Grignard reaction, Still-Gennari olefination, Pd-cat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92c866ebdda9cc68f128149ccafda749
https://doi.org/10.1002/slct.201601076
https://doi.org/10.1002/slct.201601076
Publikováno v:
Organicbiomolecular chemistry. 16(22)
A synthetic study of the construction of the C1–C23 fragment of prorocentin-4, a novel linear polyketide, is described. The synthetic highlights include the acid catalyzed epoxide opening, Gilman reaction, Pd(OH)2 catalyzed transformation of a prim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d0dac4a66a2cedb644e33463f979193
https://pubmed.ncbi.nlm.nih.gov/29796520
https://pubmed.ncbi.nlm.nih.gov/29796520
Publikováno v:
Synthesis. 47:2860-2868
A stereoselective synthesis of the complete C1–C16 framework of tianchimycins A and B is described. Key transformations include Horner–Wadsworth–Emmons, Evans aldol, Gilman’s and stereoselective alkylation reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d0230a644bd8b7fddb2ae7a8941f80f
https://doi.org/10.1055/s-0034-1378739
https://doi.org/10.1055/s-0034-1378739
Publikováno v:
Synthesis. 47:330-342
The first total synthesis of pectinolides D and E and total synthesis of pectinolides A and C was achieved from a hitherto unknown common key building block prepared from readily available d -mannitol. Key reactions involved in the synthesis are Red-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::690678af5b381570dbd0bc28e33646b8
https://doi.org/10.1055/s-0034-1378912
https://doi.org/10.1055/s-0034-1378912
Publikováno v:
Synthesis. 45:651-654
An efficient total synthesis of pectinolide H was achieved by using alkynylation, asymmetric reduction in the presence of a Corey–Bakshi–Shibata catalyst, and a Still–Gennari olefination as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a96030a2a7289d23bfc3a02a2f76a40
https://doi.org/10.1055/s-0032-1318000
https://doi.org/10.1055/s-0032-1318000
Publikováno v:
Organicbiomolecular chemistry. 13(42)
The first stereoselective total synthesis of (+)-goniothalesacetate and total synthesis of several bioactive styryl lactones, (+)-altholactone, (+)-gonioheptolide A, and (-)-goniofupyrone have been achieved from an advanced intermediate, which can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4aab12a83949d99d06c00a7cc33f57f
https://pubmed.ncbi.nlm.nih.gov/26329987
https://pubmed.ncbi.nlm.nih.gov/26329987
Publikováno v:
Tetrahedron Letters. 54:1097-1099
The first stereoselective synthesis of pectinolide C and synthesis of pectinolide A, from easily accessible 1-hexyne and d -mannitol are reported in a convergent manner. The salient features include acetylenic addition to the chiral aldehyde and Stil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2207515eba64d0963ac8f47d592b9a50
https://doi.org/10.1016/j.tetlet.2012.12.039
https://doi.org/10.1016/j.tetlet.2012.12.039