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·1552· 精细化工 FINE CHEMICALS 第 37 卷

spirocyclopropanation of barbiturate-based olefins with benzyl [39] GAZZEH H, BOUDRIGA S, ASKRI M, et al. Stoichiometry-
chlorides[J]. Synthesis, 2019, 51(4): 899-906. controlled cycloaddition of nitrilimines with unsymmetrical
[20] MALLICK R K, DUTTA S, VANJARI R, et al. Thioarylative radical exocyclic dienones: Microwave-assisted synthesis of novel mono-
cyclization of yne-dienone[J]. Journal of Organic Chemistry, 2019, and dispiropyrazoline derivatives[J]. RSC Advances, 2016, 6(55):
84(16): 10509-10517. 49868-49875.
[21] DONG J H, XIN S, WANG Y Q, et al. In situ generation and [40] SCADENG O, WEST F G. Ready access to alkylidenecyclopenten-
reactions of p-(trifluoromethyl) benzyl electrophiles: An efficient ones by Nazarov cyclization/β-Elimination of 2-hydroxyalkyl-1,
access to p-(trifluoromethyl) benzyl compounds[J]. Chemical 4-dien-3-ones[J]. European Journal of Organic Chemistry, 2014,
Communications, 2017, 53(10): 1668-1671. 2014(9): 1860-1865.
[22] FENG T, TIAN M M, ZHANG X Y, et al. Tunable synthesis of [41] WU Y K, WEST F G. Formal homologous Aldol reactions:
functionalized cyclohexa-1,3-dienes and 2-aminobenzophenones/ Interrupting the Nazarov cyclization via carboalkoxylation of
benzoate from the cascade reactions of allenic ketones/allenoate with alkynes[J]. Organic Letters, 2014, 16(9): 2534-2537.
amines and enones[J]. Journal of Organic Chemistry, 2018, 83(9): [42] LI Z, BOYD R J, BURNELL D J. Computational examination of
5313-5322. (4+3) versus (3+2) cycloaddition in the interception of Nazarov
[23] ZHANG Z P, RATNIKOV M, SPRAGGON G, et al. Photoinduced reactions of allenyl vinyl ketones by dienes[J]. Journal of Organic
rearrangement of dienones and santonin rerouted by amines[J]. Chemistry, 2015, 80(24): 12535-12544.
Angewandte Chemie International Edition, 2018, 57(4): 904-908. [43] YUAN X, ZHANG S J, DU W, et al. Asymmetric Diels-Alder
[24] TAKUBO K, MOHAMED A A B, IDE T, et al. Regioselective cycloadditions of trifluoromethylated dienophiles under trienamine
rearrangement of 4,4-disubstituted 2-hydroxycyclohexa-2, 5-dienones catalysis[J]. Chemistry-A European Journal, 2016, 22(31): 11048-11052.
under deoxyfluorination conditions[J]. Journal of Organic Chemistry, [44] SHAW S, WHITE J D. Regioselective and enantioselective addition
2017, 82(24): 13141-13151. of sulfur nucleophiles to acyclic α, β, γ, δ-unsaturated dienones
[25] XIA Z L, HU J D, SHEN Z G, et al. Re 2O 7 catalyzed dienone-phenol catalyzed by an Iron(Ⅲ)-Salen complex[J]. Organic Letters, 2015,
rearrangement[J]. RSC Advances, 2015, 5(48): 38499-38502. 17(18): 4564-4567.
[26] SHARMA S, PARUMALA S K R, PEDDINTI R K. Lewis [45] WANG Z, KANG T F, YAO Q, et al. Scandium-catalyzed
acid-mediated site-selective synthesis of oxygenated biaryls from asymmetric 1, 6-addition of 3-substituted oxindoles to linear dienyl
methoxyphenols and electron-rich arenes[J]. Journal of Organic ketones[J]. Chemistry-A European Journal, 2015, 21(21): 7709-7712.
Chemistry, 2017, 82(18): 9367-9383. [46] MENG F K, LI X B, TORKER S, et al. Catalytic enantioselective 1,
[27] JADHAV A S, PANKHADE Y A, ANAND R V. Exploring gold 6-conjugate additions of propargyl and allyl groups[J]. Nature, 2016,
catalysis in a 1, 6-conjugate addition/domino electrophilic cyclization 537: 387-393.
cascade: Synthesis of cyclohepta-[b]indoles[J]. Journal of Organic [47] REXITI R, LU J, SHA F, et al. Copper-catalyzed enantioselective 1,
Chemistry, 2018, 83(15): 8615-8626. 4-conjugate addition of dialkylzinc reagents to α, β- and α, β, γ,
[28] LIU C H, XU Y L, NIU S Y, et al. Functional ionic liquids promoted δ-unsaturated ketones[J]. Tetrahedron, 2019, 75(26): 3596-3604.
double Michael reaction of benzofuran-3-one or 1-indone and [48] MORITA A, MISAKI T, SUGIMURA T. 1, 6-Addition reaction of
symmetric dienones: Construction of spiro[benzofuran-2,1′-cyclo- 5H-oxazol-4-ones to conjugated dienones catalyzed by chiral
hexane]-3-one or spiro[cyclohexane-1,2′-indene]-1′,4(3'H)-dione guanidines[J]. Chemistry Letters, 2014, 43(12): 1826–1828.
derivatives[J]. Chinese Journal of Chemistry, 2017, 35(8): 1231-1238. [49] MONDAL B, BALHA M, PAN S C. Organocatalytic asymmetric
[29] FUSCO C D, LATTANZI A. Quinine-catalysed double Michael spirocyclization reactions of cyclic 2,4-dienones with cyanoketones:
addition of malononitrile to 1, 5-disubstituted pentadien-3-ones: A Synthesis of spirodihydropyrano cyclohexanones[J]. Organic &
stereoselective route to cyclohexanones[J]. European Journal of Biomolecular Chemistry, 2019, 17(34): 7849-7853.
Organic Chemistry, 2011, 2011(20/21): 3728-3731. [50] LIN Y (林艳), LIU W Q (刘文琴), MA G Q (马广强), et al.
[30] GENDRON T, KESSEDJIAN H, DAVIOUD-CHARVET E, et al. Synthesis and characterization of trienone analogue of curcumin[J].
Diastereoselective synthesis of 2,6-diaryltetrahydrothiopyran-4-ones Chemical Reagents (化学试剂), 2016, 38(12): 1202-1204.
by phase-transfer catalysis[J]. European Journal of Organic [51] KOWALCZYK R, BORATYŃSKI P J. Stereoselective thia-Michael
Chemistry, 2015, (8): 1790-1796. 1, 4-addition to acyclic 2,4-dienones and 2-en-4-ynones[J] Advanced
[31] LIU L, DAKA P, SARKISIAN R, et al. Oxa-Diels-Alder reaction of Synthesis & Catalysis, 2016, 358(8): 1289-1295.
isatins and acyclic α, β-unsaturated methyl ketones through cooperative [52] LI Z, LI T P, FU R G, et al. Regioselective 1, 4-conjugate
dienamine and metal Lewis acid catalysis[J]. Synthesis, 2014, aza-Michael addition of dienones with benzotriazole[J]. Heterocyclic
46(10): 1339-1347. Communications, 2017, 23(4): 287-291.
[32] WANG L L, PENG L, BAI J F, et al. Highly organocatalytic [53] LI Z, XIE D M, HE J J, et al. Synthesis of 7-arylethyl-5-arylpyrazolo
asymmetric Michael-ketone aldol-dehydration domino reaction: [1,5-a]pyrimidines through an aza-Michael addition/nucleophilic
Straightforward approach to construct six-membered spirocyclic addition/1,3-hydrogen transfer cascade[J]. Journal of Chemical
oxindoles[J]. Chemical Communications, 2010, 46(42): 8064-8066. Science, 2017, 129(10): 1579-1586.
[33] WU B, CHEN J, LI M Q, et al. Highly enantioselective synthesis of [54] GABRIELE B, MANCUSO R, VELTRI L. Recent advances in the
spiro[cyclohexanone-oxindoles] and spiro[cyclohexanonepyrazol- synthesis of indanes and indenes[J]. Chemistry-A European Journal,
ones] by asymmetric cascade [5+1] double Michael reactions[J]. 2016, 22(15): 5056-5094.
European Journal of Organic Chemistry, 2012, 43(28): 1318-1327. [55] SAULNIER S, GOLOVANOV A, VASILYEV A V. A controlled
[34] LUO X Y, WANG L L, PENG L, et al. Asymmetric double Michael tandem transformation of conjugated enynones with arenes under
reaction catalyzed by simple primary amine catalysts: A superelectrophilic activation leading to aryl-substituted dienones and
straightforward approach to construct spirocyclic oxindoles [J]. indenes[J]. RSC Advances, 2016, 6(105): 103546-103555.
Chinese Journal of Chemistry, 2012, 30(5): 1185-1188. [56] SATPATHI B, WAGULDE S V, RAMASASTRY S S V. An
[35] ALMOND-THYNNE J, WHITE A J P, POLYZOS A, et al. Synthesis enantioselective organocatalytic intramolecular Morita-Baylis- Hillman
and reactions of benzannulated spiroaminals: Tetrahydrospiro- (IMBH) reaction of dienones, and elaboration of the IMBH adducts
biquinolines[J]. ACS Omega, 2017, 2(7): 3241-3249. to fluorenones[J]. Chemical Communications, 2017, 53(57): 8042-8045.
[36] FERREIRA I M, MEIRA E B, ROSSET I G. Chemoselective [57] SATPATHI B, DUTTA L, RAMASASTRY S S V. Metal- and
biohydrogenation of α, β- and α, β, γ, δ-unsaturated ketones by the hydride-free pentannulative reductive Aldol reaction[J]. Organic
marine-derived fungus penicillium citrinum CBMAI 1186 in a Letters, 2019, 21(1): 170-174.
biphasic system[J]. Journal of Molecular Catalysis B: Enzymatic, [58] SATPATHI B, DUTTA L, RAMASASTRY S S V. Phosphine- and
2015, 115: 59-65. water-promoted pentannulative Aldol reaction[J]. Organic &
[37] DOSTAGIR SK N H MD, AWASTHI M K, MUMAR A, et al. Biomolecular Chemistry, 2019, 17(6): 1547-1551.
Selective catalysis for room-temperature hydrogenation of biomass- [59] MURAKATA M, KAWASE A, KIMURA N, et al. Synthesis of
derived compounds over supported NiPd catalysts in water[J]. ACS tofogliflozin as an SGL-T2 inhibitor via construction of
Sustainable Chemistry & Engineering, 2019, 7(10): 9352-9359. dihydroisobenzofuran by intramolecular [4+2] cycloaddition[J].
[38] ISLAM M S, BARAKAT A, AL-MAJID A M, et al. Chemical Organic Process Research Development, 2019, 23(4): 548-557.
reactivity, molecular structure, spectroscopic and DFT computational [60] KIM H Y, OH K. 1,3-Dienones and 2H-pyran-2-ones from soft
studies of spiro-heterocycle incorporating furan ring[J]. Materials α-vinyl enolization of β-chlorovinyl ketones: Defined roles of
Express, 2018, 8(4): 335-344. Brönsted and Lewis base[J]. Organic Letters, 2015, 17(24): 6254-6257.