Several creative new approaches to carbocyclic ring construction using transition metals have recently been reported. Dichlorocyclopropanes such as 1 are easily prepared by the addition of dichlorocarbene to the corresponding…
A recent publication by G. Barbarella and co-workers from Bologna, Italy (J. Org. Chem. 2004, 69, 4821.DOI: 10.1021/jo035723q)reports the rapid preparation of poorly soluble unsubstituted and modified α-quinque and sexithiophenes…
Thomas Lectka of Johns Hopkins University has reported (J. PMID:24487575 Am. Chem. Soc. 2006, 128, 1810. DOI: 10.1021/ja058077g)an elegant method for the enantioselectiveα-hydroxylation of carboxylic acids. Chiral amine catalyzed condensation…
Ontaining 1 m: of 25 mM HEPES (pH 7.five), 0.three M sucrose, 10 mM CaCl2, ten mM MgCl2. Fresh Arabidopsis rosette leaves had been harvested from 4-week-old plants grown in…
N open access short article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). www.molecularmetabolism.comThese outcomes confirmed that NNT is essential for the effects of glucose and FCCP on islet NADPH. On the…
Duncan J. Wardrop of the University of Illinois, Chicago, established (Org. 529476-80-0 Chemical name Lett. 2006, 8, 3659.DOI: 10.1021/ol0609053)the five-membered ether ring of (±)-magnofargesin (3) by the addition of benzenesulfinate…
The groups of Laurent El Kaïm and Laurence Grimaud from Ecole Nationale Supérieure de Techniques Avancées in Paris have reported on the generation of quinoxaline scaffolds (Heterocycles 2007, 73, ASAP.…
K. C. Nicolaou and his group from the Scripps Research Institute have performed the total synthesis of artochamins F and H-J applying microwave heating for the key step (Angew. Chem.…
There has been a recent surge of enthusiasm for pyrrole synthesis. Stephen L. Buchwald of MIT has reported (Org. Lett. 2007, 9, 973. DOI: 10.1021/ol062978s)a clever application of his Cu-catalyzed…
Thierry Ollevier and Zhiya Li from Université Laval, Quebec, have reported on the bismuth-catalyzedSakurai reaction toward the synthesis of homoallylic alcohols (Eur. J. 1505818-73-4 web Org. Chem. 1246761-84-1 supplier 2007,…
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