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home | synthetic organic chemistry & catalysis • university of oxford synthetic organic chemistry & catalysis • university of oxford martin smith research group contact us home research themes publications martin smith our team teaching work with us we are a synthetic chemistry research group with a focus on enantioselective catalysis, the investigation and exploitation of non-covalent interactions and the synthesis of complex molecules. we are based in the chemistry research laboratory at the university of oxford news & group updates martin has a profile published in angewandte chemie - you can read it here . congratulations to the late stage functionalization team on their collaboration with ucb on light mediated sulfonylation of anilines. direct sulfonylation of anilines mediated by visible light chem. sci. 2017 , in press. october 2017: congratulations to kat (pictured far right) on winning one of the astrazeneca-sponsored prizes for her talk titled "how does enantioselective phase transfer catalysis work?" at oxford chemistry's graduate seminar. congratulations to phil and jamie on their collaboration with paul brennan , akane kawamura and justin benesch on the discovery of a potent and selective lysine demethylase inhibitor discovery of a highly selective cell-active inhibitor of kdm2/7 angew. chem. int. ed. 2017 , in press. congratulations to the late stage functionalization team on the group's recent collaboration with ucb on late-stage cyanation. a c-h cyanation of 6-ring n -containing heteraromatics chemistry eur. j. 2017 , in press. congratulations to niels, nick and lucy on the publication of the group's collaboration with rob paton on photoheterocyclization visible light photocatalysis of 6 π heterocyclization angew. chem. int. ed. 2017 , 56 , 9468 . recent papers direct sulfonylation of anilines mediated by visible light chem. sci. 2017 , in press. discovery of a highly selective cell-active inhibitor of kdm2/7 angew. chem. int. ed. 2017 , in press. visible light photocatalysis of 6 π heterocyclization angew. chem. int. ed. 2017 , 56 , 9468 . catalytic enantioselective synthesis of atropisomeric biaryls by a cation-directed o-alkylation nature chem. 2017 , 9 , 558. a cascade strategy enables a total synthesis of morphine angew. chem. int. ed. 2016 , 55 , 14306. a counterion-directed approach to the diels-alder paradigm: cascade synthesis of tricyclic fused cyclopropanes angew. chem. int. ed. 2016 , 55 , 13813 . catalytic enantioselective synthesis of c 1 and c 2-symmetric spirobiindanones through counterion-directed enolate c -acylation angew. chem. int. ed. 2016 , 55 , 13180 . catalytic enantioselective synthesis of indanes by a cation-directed 5- endo - trig cyclization nature chem. 2015 , 7 , 171. ')

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