Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sudhakar, Athe"'
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 16563-16575 (2018)
Externí odkaz:
https://doaj.org/article/67f0d9fc76bf46a69ccd60f168b9ef25
Publikováno v:
Organic Letters. 24:8109-8114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5226a3c0c831f0641a984465c73ac7cc
https://doi.org/10.1021/acs.orglett.2c02983
https://doi.org/10.1021/acs.orglett.2c02983
Publikováno v:
Tetrahedron Letters. 60:1570-1573
Collective syntheses of five spiro[4.5]decane framework bearing sesquiterpenoids, namely, α & β-vetispirenes, β-vetivone, agarospirol and hinesol as well as formal synthesis of axenol and gleenol from a readily available precursor cyclohexanone-β
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::451dd2593c446a45b5123f12ab1ff2c5
https://doi.org/10.1016/j.tetlet.2019.05.011
https://doi.org/10.1016/j.tetlet.2019.05.011
Publikováno v:
ACS Omega, Vol 3, Iss 12, Pp 16563-16575 (2018)
ACS Omega
ACS Omega
The stereoselective total synthesis of cytotoxic marine macrolide callyspongiolide has been reported. The 14-membered macrolactone ring along with Z-olefin in the molecule was constructed via an intramolecular Horner-Wadsworth-Emmons olefination in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be32750a2104f9f11afce5c85bc5fb4
https://doaj.org/article/67f0d9fc76bf46a69ccd60f168b9ef25
https://doaj.org/article/67f0d9fc76bf46a69ccd60f168b9ef25
Publikováno v:
Tetrahedron Letters. 82:153374
The first asymmetric total synthesis of the proposed structure of metacridamide B, a 17-membered macrolide with anticancer activity, has been accomplished in a highly convergent and flexible manner. The key features of our synthesis involved hydroxyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e86248e3e0021b5814ce3488dc86e7ba
https://doi.org/10.1016/j.tetlet.2021.153374
https://doi.org/10.1016/j.tetlet.2021.153374
Publikováno v:
Organic & Biomolecular Chemistry. 13:115-124
This article reported the synthesis of fully functionalized aglycone of lycoperdinoside A and B. Pd-catalyzed Stille-Migita cross coupling between E-vinyl iodide 6 and E-vinyl stannane 23 established the highly substituted E,E-diene unit present in l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa44c34e4d448a5f06359ca7e99db82
https://doi.org/10.1039/c4ob01716a
https://doi.org/10.1039/c4ob01716a
Publikováno v:
Organicbiomolecular chemistry. 14(28)
A concise synthetic strategy has been developed for the synthesis of the macrolactone core 2 of a unique polyketide callyspongiolide 1. The key features of the strategy included an Evan's asymmetric alkylation, diastereoselective Michael type alkylat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22231100801021e6b13cee8bd1506d40
https://pubmed.ncbi.nlm.nih.gov/27337038
https://pubmed.ncbi.nlm.nih.gov/27337038
Publikováno v:
The Journal of organic chemistry. 77(21)
This paper describes the formal total synthesis of (+)-neopeltolide, a cytotoxic macrolide isolated from the marine sponge Neopeltidae. The key features of the synthesis include an asymmetric Evans alkylation to fix the C9-methyl center, Jacobsen hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a044d8bcf808488f422ff518f8f1a1f4
https://pubmed.ncbi.nlm.nih.gov/23039136
https://pubmed.ncbi.nlm.nih.gov/23039136