PadwaA.Dominoreactionsofrhodium(II)carbenoidsforalkaloid synthesis [J]. Chemical Society Reviews, 2009, 38(11): 3072-3081.
[2]
Aaron M D, Eric F. Meldrum's acids and 5-alkylidene meldrum's acids in catalytic carbon-carbon bond-forming processes[J]. Accounts of Chemical Research, 2010, 43(3): 440-454.
[3]
Nazef N, Davies R D M, Greaney M F. Formal synthesis of merrilactone a using a domino cyanide 1,4-addition-aldol cyclization[J]. Organic Letters, 2012, 14(14): 3720-3723.
[4]
Tu S J, Jiang B, Jia R H, et al. An efficient one-pot, three-component synthesis of indeno[1,2-b]quinolin-9,11(6H,10H)-dione, acridine-1,8 (2H,5H)-dione and quinoline-3-carboni trile derivatives from enaminones [J]. Organic & Biomolecular Chemistry, 2006, 4(19): 3664-3668.
[5]
Zhu X T, Xu H W, Jiang B, et al. Efficient [4 + 1]/[3 + 2 + 1] biscyclizations stereoselectively yielding unprecedented polyacyclic indeno-fused xanthenes[J]. Tetrahedron Letters, 2013, 54(47): 6341-6344.
[6]
Wright C W, Phillipson J D, Awe S O, et al. Antimalarial Activity of Cryptolepine and Some Other Anhydronium Bases[J]. Phytotherapy Research, 1996, 10(4): 361-363.
[7]
Oyekan A O, Ablordeppey S Y. Effects of cryptolepine on collageninduced aggregation and on the mobilization and metabolism of arachidonic acid by rabbit platelets[J]. General Pharmacology: The Vascular System, 1993, 24(5): 1285-1290.
[8]
Kirby G C, Paine A, Warhurst D C, et al. In vitro and in vivo antimalarial activity of cryptolepine, a plant-derived indoloquinoline[J]. Phytotherapy Research, 1995, 9(5): 359-363.
[9]
Zhu H J, Gooderham N J. Mechanisms of induction of cell cycle arrest and cell death by cryptolepine in human lung adenocarcinoma A549 cells[J]. Toxicological Sciences, 2006, 91(1): 132-139.
[10]
Olajide O A, Heiss E H, Schachner D, et al. Synthetic cryptolepine inhibits DNA binding of NF-κB[J]. Bioorganic & Medicinal Chemistry, 2007, 15(1): 43-49.
[11]
Chen Y L, Chung C H, Chen P H, et al. Synthesis and cytotoxic activity evaluation of indolo-, pyrrolo-, and benzofuro-quinolin-2(1H)-ones and 6-anilinoindoloquinoline derivatives[J]. Bioorganic & Medicinal Chemistry, 2002, 10(8): 2705-2712.
[12]
Sundaram G S M, Venkatesh C, Syam Kumar U K, et al. A concise formal synthesis of alkaloid cryptotackiene and substituted 6H-indolo[2, 3-b]quinolines[J]. The Journal of Organic Chemistry, 2004, 69(17): 5760-5762.
[13]
Sayed I E, Ramzy F, William S, et al. Neocryptolepine analogues containing N-substituted side-chains at C-11: Synthesis and antischistoso micidal activity[J]. Medicinal Chemistry Research, 2012, 21(12): 4219-4229.
[14]
Tietze L F, Modi A. Multicomponent domino reactions for the synthesis of biologically active natural products and drugs[J]. Medicinal Research Reviews, 2000, 20(4): 304-322.
[15]
Tietze L F, Rackelmann N. Domino reactions in the synthesis of heterocyclic natural products and analogs[J]. Pure and Applied Chemistry, 2004, 76(11): 1967-1983.