Enantioselective addition to a prochiral ring is a powerful approach for the preparation of C-N rings in high ee. 458532-84-8 uses This is elegantly illustrated by the report (J. Org.…
Tohru Fukuyama of the University of Tokyo has recently reported (Org. Formula of Fmoc-α-Me-Gly(Pentynyl)-OH Lett. PMID:25429455 2006, 8, 5311. Price of 279236-77-0 DOI: 10.1021/ol062112m)an elegantly conceived total synthesis of (±)-morphine…
Retrosynthetic analysis of the heptacyclic ring structure of nominine (3), a representative member of the hetisine family of alkaloids, is not for the faint of heart. David Y. 334905-81-6 manufacturer…
Synthesis: Part One of Three We last reviewed organic synthesis applications of the Grubbs reaction on April 19, 2004. The (relatively) robust nature of the commercially-available catalyst and its commercial…
(-)-Terpestacin (3), isolated from Arthrinium sp. Buy157327-48-5 FA1744, inhibits the formation of syncytia by HIV-infected T cells. PMID:26644518 A key step in the total synthesis of 3 reported (J. Buy2-Chloro-5,7-difluorobenzothiazole…
The guanacastepenes, of which guanacastepene E (3) is representative, initially elicited excitement because of their activity against drug resistant bacterial strains. Although the systemic toxicity of the guanacastepenes has cooled…
The symmetrical macrodiolide (+)-SCH 351448 (4) is the only known selective activator of transcription from the low density lipoprotein receptor. The highly convergent synthesis of 4 from 1 and 2…
Larry E. Overman of the University of California, Irvine has recently (Angew. Chem. Int. PMID:25959043 2,4-Bis(trifluoromethyl)benzaldehyde supplier Ed. 2006, 45, 2912. DOI: 10.1002/anie.200600417)described the first total synthesis of the antibiotic…
(+)-Rishirilide (4), an inhibitor of α2-macroglobulin, a tetrameric serum glycoprotein that is an irreversible protease inhibitor, has a deceptively simple structure. Thomas R. R. Pettus of the University of California…
Vigulariol (3), isolated from the octocoral Vigularia juncea (Pallas), is active against human lung adenocarcinoma cells (IC50 = 18 nM). A key step in the synthesis of 3 reported (Angew.…
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