80393-27-7Relevant articles and documents
Enantioselective Synthesis of Chiral Indane Derivatives by Rhodium-Catalyzed Addition of Arylboron Reagents to Substituted Indenes
Umeda, Moeko,Noguchi, Hikaru,Nishimura, Takahiro
supporting information, p. 9597 - 9602 (2020/12/21)
Rhodium-catalyzed asymmetric addition of arylboron reagents to indene derivatives proceeded to give 2-arylindanes in good yields with high enantioselectivity. Deuterium-labeling experiments indicated that the present reaction involved a 1,4-Rh shift from an initially formed benzylrhodium to an arylrhodium intermediate before protonation leading to the corresponding addition product. The asymmetric addition was also successful for acenaphthylene, which has a similar skeleton to indene, where it was found that the benzylrhodium intermediate underwent direct protonation without the 1,4-Rh shift.
IONIC HYDROGENATION OF 1,3-INDANEDIONE DERIVATIVES
Popova, O. K.,Pernes, Z. N.,Katinkin, M. I.,Markosyan, S. M.,Kopteva, N. I.,et al.
, p. 1709 - 1711 (2007/10/02)
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