Results from our group has established the use of  stereoelectronic effects to manipulate excited state reactivity similar to ground state enantioselective transformations under organo-catalytic control. This opens up avenues to exploit the well-known stereoelectronic effects to control reactivity and selectivity for some of the most synthetically useful excited state transformations. Some of the recent publication from our group is listed below.

  1. Vallavoju, N; Sermadurai, S.; Pemberton, B. C.; Jockusch, S.; Sibi, M. P.; Sivaguru, J.* Insights into the mechanistic aspects of organo-photocatalysis mediated by thioureas. Chem., Int. Ed. 2016, 55, 5446-5451.(Selected as “important paper” and featured as a frontispiece).
  2. Kumarasamy, E.; Sibi, M. P.; Sivaguru, * Non-biaryl and hetero-biaryl atropisomers: Molecular templates with promise for atropselective chemical transformations”, Chem. Rev.,2015,115, 11239–11300.
  3. Vallavoju, N; Sermadurai, S.; Jockusch, S.; Sibi, M. P.; Sivaguru, J.* Enantioselective organo-photocatalysis mediated by atropisomeric thiourea derivatives. Angew Chem., Int. Ed., 2014, 53, 5604-5608 and Chem. 2014, 126, 5710-5714.
  4. Vallavoju, N. Sermadurai, S.; Jockusch, S.; Prabhakaran, M. T.; Sibi, M. P.; Sivaguru, J.* Evaluating thiourea architecture for intramolecular [2+2]-photocycloaddition of 4-alkenylcoumarins. Synt. Catal., 2014, 356, 2763-2768.

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