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- Role of surface phenomena in the reaction of molecular solids: the Diels–Alder reaction on pentacene. Selma Piranej, Michael A. W. Shelhart Sayers, Gregory J. Deye, Sergey N. Maximoff, Jonathan P. Hopwood, Haejun Park, Jean G. Slavsky, Jacob W. Ciszek
, CrystEngComm
, 2020
, 22
, 4108
- Regioselectivity and endo/exo selectivity in the cycloadditions of the phthalazinium dicyanomethanide 1,3-dipole with unsymmetrical alkene and alkyne dipolarophiles. Unexpected reversals of regiochemistry: a combined experimental and DFT theoretical study. Richard N. Butler, Anthony G. Coyne, Patrick McArdle, Desmond Cunningham, Luke A. Burke
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 1391
- Rhodium-catalyzed C7-alkylation of indolines with maleimides. Changduo Pan, Yun Wang, Chao Wu, Jin-Tao Yu
, Org. Biomol. Chem.
, 2018
, 16
, 693
- Macrocyclic multinuclear metal complexes acting as catalysts for organic synthesis. Bikash Dev Nath, Kazuto Takaishi, Tadashi Ema
, Catal. Sci. Technol.
, 2020
, 10
, 12
- Cavity-based applications of metallo-supramolecular coordination cages (MSCCs). Sarita Yadav, Palanisamy Kannan, Guanyinsheng Qiu
, Org. Chem. Front.
, 2020
, 7
, 2842
- Catalytic reactions within the cavity of coordination cages. Yu Fang, Joshua A. Powell, Errui Li, Qi Wang, Zachary Perry, Angelo Kirchon, Xinyu Yang, Zhifeng Xiao, Chengfeng Zhu, Liangliang Zhang, Feihe Huang, Hong-Cai Zhou
, Chem. Soc. Rev.
, 2019
, 48
, 4707
- Pd(ii)-Catalyzed oxidative alkenylation of 4-hydroxycoumarin with maleimide via a C–H bond activation strategy. Kumud Sharma, Kashmiri Neog, Abhilash Sharma, Pranjal Gogoi
, Org. Biomol. Chem.
, 2021
, 19
, 6256
- Regioselective C–H alkylation and alkenylation at the C5 position of 2-amino-1,4-naphthoquinones with maleimides under Rh(iii) catalysis. Prasanna Anjaneyulu Yakkala, Deepesh Giri, Bharatkumar Chaudhary, Prashant Auti, Satyasheel Sharma
, Org. Chem. Front.
, 2019
, 6
, 2441
- Steric Reversal of the
endo-Selectivity Effect in 1,3-Dipolar Cycloadditions of Phthalazinium-2-ylides with N-Substituted Maleimides: endo- and exo-1,2-(Dicarboxy-N-substituted imido)-1,2,3,10b-tetrahydropyrrolo[2,1-a]phthalazines†. Richard N. Butler, Derval M. Farrell
, J. Chem. Res. (S)
, 1998
, 214
- endo/exo Facial selectivities in cycloaddition reactions of substituted 1,2,3-triazolium-1-methanides, unstabilised 1,3-dipoles, with some alkene dipolarophiles: models for 1,2,3-triazolium-1-aminides: new tetracyclic pyrrolo[1,2-c][1,2,3]benzotriazole structures: azolium 1,3-dipoles. R. N. Butler, Leonie M. Wallace
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 1778