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- Overcrowded molecules. Part III. The synthesis and photorearrangement reactions of 2,3-bisdiphenylmethylene-1-indanone and 4b,5-dihydro-5,5,10-triphenyl-11-diphenylmethylene-11H-benzo[b]fluorene. H. G. Heller, D. Auld, K. Salisbury
, J. Chem. Soc. C
, 1967
, 2457
- Overcrowded molecules. Part IV. Thermal and photochemical electrocyclic reactions of trans-2-benzylidene-1-diphenylmethyleneindane and its 3-methyl derivative. H. G. Heller, K. Salisbury
, J. Chem. Soc. C
, 1970
, 399
- Charge-transfer complexes of some 5-membered heterocyclics and their annellated derivatives with tetracyanoethylene. A. R. Cooper, C. W. P. Crowne, P. G. Farrell
, Trans. Faraday Soc.
, 1966
, 62
, 18
- Overcrowded molecules. Part I. 1,2-Bisdiphenylmethyleneindane and 1,2-bisdiphenylmethylene-3,3-dimethylindane. H. G. Heller, D. Auld, K. Salisbury
, J. Chem. Soc. C
, 1967
, 682
- Gas-phase thermochemistry of polycyclic aromatic hydrocarbons: an approach integrating the quantum chemistry composite scheme and reaction generator. Irina Minenkova, Arseniy A. Otlyotov, Luigi Cavallo, Yury Minenkov
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 3163
- A symmetry-allowed pericyclic reaction involving two ‘forbidden’ processes. The thermal rearrangement of (E)-2-benzylidene-(Z)-mesityl(phenyl)-methyleneindane into (Z)-2-benzyl-1-mesityl(phenyl)methyleneindene. John S. Hastings, Harry G. Heller, Howard Tucker, Keith Smith
, J. Chem. Soc., Chem. Commun.
, 1974
, 348
- Colour-responsive fluorescent oxy radical sensors. Baris Yucel, Bahar Sanli, Huseyin Akbulut, Suheyla Ozbey, Andrew C. Benniston
, Org. Biomol. Chem.
, 2012
, 10
, 1775
- Index of subjects, 1967
, J. Chem. Soc. C
, 1967
, 2729
- 183. The interaction of diphenylketen and 2-benzylideneindan-1-one. Neil Campbell, P. S. Davison, H. G. Heller
, J. Chem. Soc.
, 1963
, 993
- Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons. Bingjian Gao, Suchen Zou, Guoqing Yang, Yongzheng Ding, Hanmin Huang
, Chem. Commun.
, 2020
, 56
, 12198