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118Jörn Piel.
Biosynthesis of polyketides by trans-AT polyketide synthases, Nat. Prod. Rep., 2010, 27, 996. Xiao-Ming Zhang, Yong-Qiang Tu, Yi-Jun Jiang, Yong-Qiang Zhang, Chun-An Fan and Fu-Min Zhang.
Tandem reactions of cis-2-acyl-1-alkynyl-1-aryl cyclopropanes tuned by gold(i) and silver(i) catalysts: efficient synthesis of pyran-fused indene cores and 2,4,6-trisubstituted phenols, Chem. Commun., 2009, 4726. Gregory W. O’Neil and Alois Fürstner.
B-AlkylSuzuki couplings for the stereoselective synthesis of substituted pyrans, Chem. Commun., 2008, 4294. Yvonne K. Booth, William Kitching and James J. De Voss.
Biosynthesis of insect spiroacetals, Nat. Prod. Rep., 2009, 26, 490. Nadale K. Downer-Riley and Yvette A. Jackson.
Synthesis highlights, Annu. Rep. Prog. Chem., Sect. B: Org. Chem., 2009, 105, 167. Salama Omar and Leif A. ErikssonPresent address: School of Chemistry, National University of Ireland, Galway, Ireland..
Computational study of khellin excited states and photobinding to DNA, Photochem. Photobiol. Sci., 2009, 8, 1179. Damien Thompson, Simon Coleman, Dermot Diamond and Robert Byrne.
Electronic structure calculations and physicochemical experiments quantify the competitive liquid ion association and probe stabilisation effects for nitrobenzospiropyran in phosphonium-based ionic liquids, Phys. Chem. Chem. Phys., 2011, 13, 6156. A. Jonathan Singh, Mina Razzak, Paul Teesdale-Spittle, Thomas N. Gaitanos, Anja Wilmes, Ian Paterson, Jonathan M. Goodman, John H. Miller and Peter T. Northcote.
Structure–activity studies of the pelorusides: new congeners and semi-synthetic analogues, Org. Biomol. Chem., 2011, 9, 4456. Gullapalli Kumaraswamy, Neerasa JayaprakashN.J. and G.B. made equal contributions to this work and Guniganti Balakishan.
Cu(i)-catalyzed tandem benzyldiazoester coupling with terminal alkyne–allene formation–Michael reaction: Application to the syntheses of oxa and azacycles, Org. Biomol. Chem., 2011, 9, 7913. Muhammad Ashram, David O. Miller and Paris E. Georghiou.
Chemical reactivity of hydroxymethylnaphthols: hetero-Diels–Alder products of o-naphthoquinomethides derived from 2- and 3-hydroxymethylnaphthols, J. Chem. Soc., Perkin Trans. 1, 2002, 0, 1470.