Unusual traits of cis and trans-2,3-dibromo-1,1-dimethylindane on the way from 1,1-dimethylindene to 2-bromo-, 3-bromo-, and 2,3-dibromo-1,1-dimethylindene

Rudolf Knorr, David S. Stephenson, Ernst Lattke, Petra Böhrer and Jakob Ruhdorfer
Beilstein J. Org. Chem. 2016, 12, 1178–1184. https://doi.org/10.3762/bjoc.12.113

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Supporting Information File 1: Alternative synthetic routes to 1,1-dimethylindene (2) and congeners; experimental procedures for 2, 1,1-dimehylindane (9), 3-methyl-1-phenylbutan-2-ol, N-(1,1-dimethylindan-3-ylidene)hydrazine, and N,N´-bis(1,1-dimethylindan-3-ylidene)hydrazine.
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Unusual traits of cis and trans-2,3-dibromo-1,1-dimethylindane on the way from 1,1-dimethylindene to 2-bromo-, 3-bromo-, and 2,3-dibromo-1,1-dimethylindene
Rudolf Knorr, David S. Stephenson, Ernst Lattke, Petra Böhrer and Jakob Ruhdorfer
Beilstein J. Org. Chem. 2016, 12, 1178–1184. https://doi.org/10.3762/bjoc.12.113

How to Cite

Knorr, R.; Stephenson, D. S.; Lattke, E.; Böhrer, P.; Ruhdorfer, J. Beilstein J. Org. Chem. 2016, 12, 1178–1184. doi:10.3762/bjoc.12.113

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