Ed in Amaryllidaceae alkaloids synthesis have been identified for the very first time and are worthyFigure 6. Distribution of putative single nucleotide polymorphisms (SNP) in the transcriptome of L. aurea.…
Luigino Troisi of the University of Salento found (Tetrahedron Lett. 2010, 51, 371. DOI: 10.1016/j.tetlet.2009.11.023) that a variety of primary and secondary amines could be coupled with a benzylic halide…
Lew Mander of the Australian National University recently reported (J. Am. Chem. PMID:33679749 Soc. 2003, 125, 2400.DOI: 10.1021/ja029725o)the total synthesis of the pentacyclic alkaloid GB 133, which had been isolated…
Alessandro Palmieri of the University of Camerino developed (Synlett 2010, 2468. DOI: 10.1055/s-0030-1258031) the condensation of a nitro acrylate 1 with a 1,3-dicarbonyl partner 2 to give the furan 3.…
Masahito Ochiai developed ( 2008, March 24) the iodosobenzene-mediated cleavage of alkenes to keto aldehydes. PMID:23557924 Thottumkara K. Vinod of Western Illinois University described (Org. Lett. 2010, 12, 5640. DOI:…
Barry M. 6-Bromo-3-chloroisoquinoline structure Trost of Stanford University generated (J. Am. Chem. Soc. 2011, 133, 4766. DOI: 10.1021/ja200971v) a β-keto carbene from the propargyl alcohol 1, leading to the cyclopropane…
Jon D. Stewart of the University of Florida established (Chem. Commun. 2010, 46, 8558. DOI: 10.1039/C0CC03119D) a scalable enzymatic reduction of geranial 1 to citronellal 2. Andreas S. Bommarius of…
(Taylor), Goniothalesdiol A (Xie/She), (-)-7-Deoxyloganin (Lupton), (-)-Apicularen A (Uenishi)L-783, 277 (Banwell) In the course of a synthesis of (-)-Sclerophytin A (3), James P. Morken of Boston College showed (J. Am.…
Ts, D. M.; Myagkota, S. V. J. Phys. Chem. Solids 2008, 69, 2520-2526. (18) Stoumpos, C. C.; Malliakas, C. D.; Kanatzidis, M. G. Inorg. Chem. 2013, 52, 9019-9038. (19) Babin,…
:0 i18:0 18:0 P MUFA 16:1n-7c 17:1n-8ca 18:1n-9c 18:1n-7c 20:1n-9c 24:1n-9c P PUFA P n-3 20:5n-3 (EPA) 22:6n-3 (DHA) 22:5n-3 P n-6 20:4n-6 (AA) 22:5n-6 22:4n-6 n-3/n-6 39.1 (0.7) 13.8…
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