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1 CHCF3] or 1-trifluoromethylated indanes (CF3-indanes).
2 raction-decarbonylation-ISC recloses to give indan.
3 how similar efficiency in the preparation of indanes.
4 tric synthesis of 2,3-dihydrobenzofurans and indanes.
5 ed to prepare optically active 1-substituted indanes.
6 r; they may form both CF3-alkenes and/or CF3-indanes.
7 Here we show that 2-pyridine-3-yl-methylene-indan-1,3-dione (PRT4165) is a potent inhibitor of PRC1-
10 that 4-(2-butyl-6, 7-dichloro-2-cyclopentyl-indan-1-on-5-yl) oxobutyric acid (DCPIB), a potent volum
11 lar carboamination reactions, which afford 2-indan-1-ylpyrrolidines that result from syn-addition, ar
12 zed carboetherification of alkenes affords 2-indan-1-yltetrahydrofuran products in moderate to good y
13 where Aic(NN) is 2-amino-5-nitronylnitroxide-indan-2-carboxylic acid, have been inserted at positions
16 ]p yrazolo[1,5-a]pyrimidine-7-carbonyl}amino)indan-5-carboxylic acid (1), that is uniquely suited as
18 roach for the synthesis of amino-substituted indanes and tetralins from readily available alkyne-deri
22 tio- and diastereoselective route to complex indanes bearing all-carbon quaternary stereogenic centre
28 t arising either from nucleophilic addition (indanes) or loss of a proton beta to the indanyl-type ca
29 e formation and identified the hydrolysis of indan oxide as a key step in maximizing the production o
30 These results confirmed the significance of indan oxide formation and identified the hydrolysis of i
31 ugh a monooxygenase activity forming (1S,2R)-indan oxide, with no dehydrogenation of trans-(1R,2R)-in
32 placement of substituted benzyl groups by an indan rigid moiety in a previously described N-indazole-
33 eatures included the direct synthesis of the indan skeleton and the radical addition to a quinone.
34 domino reaction for the synthesis of diverse indanes starting from simple cinnamic acid esters is des
35 U-99194A [5, 6-dimethoxy-2-(di-n-propylamino)indan], suggesting that activation of the BDNF pathway v
36 bond activation approach to the synthesis of indans, tetralins, dihydrofurans, dihydroindoles, and ot
37 aphthalene oxide (254 nm) was reexamined and indan was found to be a primary photoproduct, as well as
38 ctivity of naturally occurring and synthetic indanes, we have synthesized a novel indane scaffold tha
39 herein summarize the asymmetric syntheses of indanes with a particular focus on asymmetric catalysis,
40 s (pseudocumene, mesitylene) afford only CF3-indanes with a predominantly cis-orientation of substitu
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