105678-94-2Relevant articles and documents
One-pot electrosynthesis of 2,3-bis(spiro-2-indanyl-1,3-dione)-indeno[1,2-b]furan-4-one
Horcajada, Roberto,Batanero, Belen,Barba, Fructuoso,Martín, Avelino
, p. 6437 - 6441 (2007)
The 2,3-bis(spiro-2-indanyl-1,3-dione)-indeno[1,2-b]furan-4-one has been synthesized by cathodic reduction of 2,2-dibromo-1,3-indandione in dichloromethane-Bu4NBF4. In contrast, tris-indanedione was the main product when acetonitrile
Synthesis of 2,3-diaryl-2,3,4,4а-tetrahydro-5Н-indeno[1,2-c]pyridazin-5-ones
Chagarovskiy, Alexey O.,Strel’tsova, Elena D.,Rybakov, Victor B.,Levina, Irina I.,Trushkov, Igor V.
, p. 240 - 245 (2019)
[Figure not available: see fulltext.] The reaction of 1,3-indanedione-derived donor-acceptor cyclopropanes with phenylhydrazine in the presence of catalytic amounts of scandium trifluoromethanesulfonate leads to the formation of indeno[1,2-c]pyridazine de
N-Iodosuccinimide-Initiated Spirocyclopropanation of Styrenes with 1,3-Dicarbonyl Compound for the Synthesis of Spirocyclopropanes
Qian, Ping,Du, Bingnan,Song, Ruichun,Wu, Xiaodong,Mei, Haibo,Han, Jianlin,Pan, Yi
, p. 6546 - 6553 (2016/08/16)
Herein is reported an N-iodosuccinimide-initiated spirocyclopropanation reaction of styrenes with 1,3-dicarbonyl compounds in the presence of white LED light. The reaction proceeds via two C-H and two C-I bond cleavage event, along with two C-C bond forma
