Publisher
International Union of Crystallography (IUCr)
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Cited by
5 articles.
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1. Carbenoid-mediated nucleophilic “hydrolysis” of 2-(dichloromethylidene)-1,1,3,3-tetramethylindane with DMSO participation, affording access to one-sidedly overcrowded ketone and bromoalkene descendants§;Beilstein Journal of Organic Chemistry;2014-01-31
2. Ideal Molecular Conformation versus Crystal Site Symmetry;Crystal Growth & Design;2012-07-24
3. Front strain in the structure of 2-benzylidene-1,1,3,3-tetramethylindan, a sterically congested styrene;Acta Crystallographica Section C Crystal Structure Communications;1992-03-15
4. Sterically congested molecules. Part 4. Front strain along a C–C double bond in the crystal structure of [1-(1,1,3,3-tetramethylindan-2-ylidene)-1-(trimethylsilyl)methyl] 2-trimethylsilylphenyl thioether;J. Chem. Soc., Perkin Trans. 2;1992
5. 2,2,2',2',5,5,5',5'-Octamethyl-2,2',5,5'-tetrahydrofulvalene,C18H28;Acta Crystallographica Section C Crystal Structure Communications;1985-01-15