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0342553400
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Quite recently, the successful synthesis of chiral tetranuclear molecular squares has been reported
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Quite recently, the successful synthesis of chiral tetranuclear molecular squares has been reported: Anderson, S.; Neidlein, U.; Gramlich, V.; Diederich, F. Angew. Chem., Int. Ed. Engl. 1995, 34, 1596.
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0000209427
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A spiro building unit (racemic) has recently been applied to the synthesis of molecular squares: Small
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A spiro building unit (racemic) has recently been applied to the synthesis of molecular squares: Small, J. H.; McCord, D. J.; Greaves, J.; Shea, K. J. J. Am. Chem. Soc. 1995, 117, 11588.
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33744639870
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1 symmetry has been attained by way of the palladium-catalyzed intramolecular Heck-type arylations
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1 symmetry has been attained by way of the palladium-catalyzed intramolecular Heck-type arylations:
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20
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33744588757
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For intramolecular hydrosilation, see
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For intramolecular hydrosilation, see:
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23
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85027864497
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33744682398
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Throughout the paper, the absolute configuration of the silicon central chirality is shown first with a subscript Si. The difference in the absolute configurations of silicon between 1 and the precursors is merely due to the priority sequence.
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Throughout the paper, the absolute configuration of the silicon central chirality is shown first with a subscript Si. The difference in the absolute configurations of silicon between 1 and the precursors is merely due to the priority sequence.
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30
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33744657717
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The absolute configurations at the silicon atom in 1 are named according to the central chirality notation.1
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The absolute configurations at the silicon atom in 1 are named according to the central chirality notation.1
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31
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For the synthesis and X-ray structures of SILOPs and their Rh(l) complexes, see: Tamao, K.; Nakamura, K.; Yamaguchi, S.; Shiro, M.; Saito, S. Chem. Lett. 1996, 1007.
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33744686370
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2, 2 mol %; Rh/DIOP = 1:1), the reaction did not go to completion at -20 °C even after 7 days.
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2, 2 mol %; Rh/DIOP = 1:1), the reaction did not go to completion at -20 °C even after 7 days.
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