Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Rodney A, Fernandes"'
Publikováno v:
Chemical Communications. 59:2007-2010
A stereodivergent protecting-group-directed Tsuji–Trost cyclization with efficient access to both 2,5-cis- and 2,5-trans-disubstituted-THF scaffolds has been realized with extension to the total synthesis of oxylipids and (+)-petromyroxol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eecc08d67682115d509a472bcc5ddbbe
https://doi.org/10.1039/d2cc04579f
https://doi.org/10.1039/d2cc04579f
Autor:
Rodney A. Fernandes, Ashvin J. Gangani
Publikováno v:
Organic Letters. 24:7400-7404
An oxidant dependent switchable palladium-catalyzed synthesis of 1,3-oxazines and benzohydrazonates (azines) from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ee879f94b88a4579c6abc97cf2c853
https://doi.org/10.1021/acs.orglett.2c02942
https://doi.org/10.1021/acs.orglett.2c02942
Autor:
Rodney A. Fernandes, Naveen Chandra
Publikováno v:
Synthesis. 54:4049-4058
Concise and efficient protecting-group-free total syntheses of chatenaytrienins-1, -3, -4 and muridienins-1–4 have been achieved. The key steps involve ring-closing metathesis (RCM) and C(sp)–C(sp3)-Sonogashira coupling. This work reports the fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b76747452a81dce4e3b998d4880b97b
https://doi.org/10.1055/a-1828-5837
https://doi.org/10.1055/a-1828-5837
Publikováno v:
Organic & Biomolecular Chemistry. 20:427-443
This paper discloses the efficient palladium-catalyzed anti-Markovnikov oxidative acetalization of activated terminal olefins with iron(III) sulfate as the reoxidant. This methodology requires mild reaction conditions and shows high regioselectivity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a944be3b67284d4b48a2c726adb5b3ed
https://doi.org/10.1039/d1ob02227j
https://doi.org/10.1039/d1ob02227j
Publikováno v:
The Journal of Organic Chemistry.
An efficient diastereoselective allylation of aldehydes with functionalized allyl bromolactone paved an excellent path toward the protecting-group-free divergent total synthesis of various guaianolides (+)-ligustrin, (+)-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c996c5a2acaccf7f87f655fcc709d1b
https://doi.org/10.1021/acs.joc.2c02094
https://doi.org/10.1021/acs.joc.2c02094
Publikováno v:
Chemistry, an Asian journal. 17(23)
A Ni(II)- and Co(II)-catalyzed sequential iodination of sulfonamides using inexpensive and milder molecular iodine (I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26353fa400385a97ac7a5cd2c9317a1b
https://pubmed.ncbi.nlm.nih.gov/36215206
https://pubmed.ncbi.nlm.nih.gov/36215206
Publikováno v:
Organic Letters. 23:6227-6231
An efficient method for the synthesis of 5-vinyl-2-isoxazolines by Pd-catalyzed intramolecular O-allylation of ketoximes has been developed. The reaction involves Pd(0)-catalyzed π-allyl formation via leaving group ionization or Pd(II)-catalyzed all
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43d41f4fc7079e5963791f1a926e68a1
https://doi.org/10.1021/acs.orglett.1c01897
https://doi.org/10.1021/acs.orglett.1c01897
Publikováno v:
The Journal of organic chemistry.
An efficient method for the synthesis of (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d24bfc384a27ee31fb7070761d30a6e
https://pubmed.ncbi.nlm.nih.gov/35895934
https://pubmed.ncbi.nlm.nih.gov/35895934
Publikováno v:
New Journal of Chemistry. 45:18976-18982
A concise stereoselective total synthesis of two diastereomeric obolactones and 7′,8′-dihydroobolactones has been achieved using a metal-free catalytic δ-hydroxyalkynone rearrangement, which could provide the required dihydro-γ-pyrone moiety. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::442f2155e8e767fa6f305f0051ae3432
https://doi.org/10.1039/d1nj03990c
https://doi.org/10.1039/d1nj03990c
Publikováno v:
European Journal of Organic Chemistry. 2021:711-740
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c688d755ca4d59adeea53b259dcfe1c7
https://doi.org/10.1002/ejoc.202001246
https://doi.org/10.1002/ejoc.202001246