ライフサイエンスコーパス: isoindole

1 ne-diene to generate the target hexahydro-1H-isoindole.

2 ne, and cyanide, yielding a fluorescent beta-isoindole.

3 tment with 2-(4-methyl-phenyl)sulphanyl-1 H -isoindole-1,3(2 H )-dione 6b.

4 (2,4-Difluoro-phenyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3(2H)-dione (CPS49) is a member of a recentl

5 Thalidomide, 2-(2,6-dioxo-3-piperidinyl)-1H-isoindole-1,3(2H)-dione, has been shown to inhibit angio

6 on of o-halobenzoates produces 2-substituted isoindole-1,3-diones in good yields.

7 ydropyridazino[4',5':1,2]indolizino[3,4,5-ab]isoindole-1,4-dione 11.

8 (1E)-(4-ethoxyphenyl) methylene] amino}spiro[isoindole-1,9'-xanthen]-3(2H)-one (DEMAX) for Al(III) ch

9 d 14-15, benzo[1',2'-1,2]indolizino[3,4,5-ab]isoindoles 10, pyridazino[4',5':1,2]indolizino[3,4,5-ab]

10 10, pyridazino[4',5':1,2]indolizino[3,4,5-ab]isoindoles 12-13, and 2,3-hydropyridazino[4',5':1,2]indo

11 They are indolizino[3,4,5-ab]isoindoles 2-9 and 14-15, benzo[1',2'-1,2]indolizino[3,4

12 igh as 10(4) cd/m(2) and indolizino[3,4,5-ab]isoindole 3 emits beautifully blue light.

13 (2), with 1-imino-4,7-bis(1-methylethoxy)-1H-isoindole-3-amine (4).

14 ines, azepanes, N-substituted 2,3-dihydro-1H-isoindoles, 4,5-dihydropyrazoles, pyrazolidines, and 1,2

15 ch higher binding affinities than the parent isoindoles (5a-e), and whereas 7a-c were agonists in the

16 chemistry of the ring junction of the benz[e]isoindole and a two-carbon spacer chain were optimal.

17 ew of the reported synthetic methods towards isoindoles and related heteroaromatic systems over a tim

18 4-Cl-L-Thr, N-derivatization as fluorescent isoindoles, and HPLC separation compared with authentic

19 However, isoindoles are relatively unstable 10pi-heteroaromatic s

20 ist, a novel series of 6-OMe hexahydrobenz[e]isoindoles attached to a bicyclic heterocyclic moiety vi

21 ificantly, spontaneous polymerization of the isoindole by-product generates colored derivatives, prov

22 ion for the chiral separation of cyanobenz[f]isoindole (CBI) derivatives of amino acids was developed

23 Isoindole containing BODIPY dyes are highly fluorescent

24 ineered cysteine on the substrate to form an isoindole cross-linked product could not be performed in

25 First, the time-dependent degradation of the isoindole derivative L-serine-NDA-beta-mercaptoethanol w

26 The isoindole derivative was observed to react further with

27 was derivatized with OPA to form a UV-active isoindole derivative which was then detected at 230 nm.

28 nt lactam form of the originally fluorescent isoindole derivative.

29 be measured by formation of the fluorescent isoindole derivatives of these compounds.

30 ed for the concise synthesis of hexahydro-1H-isoindole derivatives starting from phenacyl bromides.

31 -2-ones with N-substituted maleimides toward isoindole derivatives through the reaction sequence cycl

32 ne along with amperometric monitoring of the isoindole derivatives.

33 ng occurred at these positions to produce an isoindole fluorophore in the wild-type mu receptor.

34 anines, metal containing cyclic tetramers of isoindole, form coordination complexes with most element

35 The kinetics of isoindole formation resulting from covalent binding of N

36 The fluorescence of the benzo[f]isoindole formed upon cross-linking of mu-opioid recepto

37 The formation of the isoindole goes to 85% completion and the overall recover

38 Over the past few years, isoindoles have found wide application in materials scie

39 e unimolecular degradation of the protonated isoindole in the absence of solvent or atmosphere, sugge

40 ctional calculations for indolizino[3,4,5-ab]isoindole (INI) derivatives.

41 cycloaddition reactions between pyrido[2,1-a]isoindole (PIS) and acetylene or ethylene derivatives.

42 highly specific requirements for the benz[e]isoindole portion and linker chain, a wide variety of tr

43 annelation of the [1,2]oxazole moiety to the isoindole ring, producing derivatives with a wide substi

44 ol to form a more stable fluorescent methoxy-isoindole, shedding new light on the basis for enhanced

45 of 22 derivatives of the [1,2]oxazolo[5,4-e]isoindole system were synthesized through an efficient a

46 a novel series of tricyclic hexahydrobenz[e]isoindoles was synthesized.