Abstract:°All compounds exhibited IR and NMR spectra consistent with the assigned structure.b There were four rats per group in each experiment. c Yield of analytically pure material; yields were not optimized. d C, H, and N analyses were within ±0.4% of theoretical values for the formulas given. ® Means ± SE; all results were analyzed for statistically significant differences from control values using analysis of variance; nonsignificant values (p > 0.05) are indicated by an asterisk, f Decomposition. g Toxic at 50 mg… Show more
“…The reaction of cyclic imine 5e afforded the mono-fluorinated cycloadduct 6e in 52% yield by a sequence of the cycloaddition followed by dehydrofluorination of the corresponding difluorinated cycloadduct (entry 5). The arylquinolizine ring system is common in many naturally occurring alkaloids. , The interesting biological activities of many of these compounds and their derivatives have promoted considerable effort directed toward the construction of this system 2 Lewis Acid Catalyzed Hetero Diels−Alder Reactions of 2b with Imines a Isolated yields from α,β-unsaturated ketone 3b . …”
A Mg(0)/Me 3 SiCl system was found to be effective for the preparation of difluoro Danishefsky's dienes 2, which involves selective C−F bond cleavage of trifluoromethyl ketones 3. Subsequent hetero Diels−Alder reactions of 2 with aldehydes and imines gave a variety of fluorinated six-membered heterocycles.
“…The reaction of cyclic imine 5e afforded the mono-fluorinated cycloadduct 6e in 52% yield by a sequence of the cycloaddition followed by dehydrofluorination of the corresponding difluorinated cycloadduct (entry 5). The arylquinolizine ring system is common in many naturally occurring alkaloids. , The interesting biological activities of many of these compounds and their derivatives have promoted considerable effort directed toward the construction of this system 2 Lewis Acid Catalyzed Hetero Diels−Alder Reactions of 2b with Imines a Isolated yields from α,β-unsaturated ketone 3b . …”
A Mg(0)/Me 3 SiCl system was found to be effective for the preparation of difluoro Danishefsky's dienes 2, which involves selective C−F bond cleavage of trifluoromethyl ketones 3. Subsequent hetero Diels−Alder reactions of 2 with aldehydes and imines gave a variety of fluorinated six-membered heterocycles.
Reported is the controllable selectivity syntheses of four distinct products from the same starting materials by visible-light photoredoxcatalysis.Byemploying adicyanopyrazine-derived chromophore (DPZ) as photoredoxcatalyst, an aerobic radical mechanism has been developed, and allows the reactions of N-tetrahydroisoquinolines (THIQs) with Nitaconimides to through four different pathways,i ncluding addition-cyclization, addition-elimination, addition-coupling, and addition-protonation, with satisfactory chemoselectivity. The current strategy provide straightforwarda ccess to four different but valuable N-heterocyclic adducts in moderate to excellent yields.
Molecular motions are ubiquitous in nature and they immutably play intrinsic roles in all actions. However, exploring appropriate models to decipher molecular motions is an extremely important but very challenging task for researchers. Considering aggregation‐induced emission (AIE) luminogens possess their unique merits to visualize molecular motions, it is particularly fascinating to construct new AIE systems as models to study molecular motion. Herein, a novel quinolizine (QLZ) AIE system was constructed based on the restriction intramolecular vibration (RIV) mechanism. It was demonstrated that QLZ could act as an ideal model to visualize single‐molecule motion and macroscopic molecular motion via fluorescence change. Additionally, further elaborate tailoring of this impressive core achieved highly efficient reactive oxygen species production and realized fluorescence imaging‐guided photodynamic therapy applications, which confirms the great application potential of this new AIE‐active QLZ core. Therefore, this work not only provides an ideal model to visualize molecular motion but also opens a new way for the application of AIEgens.
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