Citation: Gao Dongmei, He Chunting, Zhang Tao, Du Zhenting. Progress in Syntheses of 6H-dibenzo[b,d] pyran-6-one and Its Derivatives[J]. Chemistry, 2019, 82(8): 731-736.
6H-二苯并[b,d]吡喃-6-酮及其衍生物的合成方法研究进展
-
关键词:
- 6H-二苯并[b,d]吡喃-6-酮
- / 碳氢活化
- / 分子内关环
- / 联苯
English
Progress in Syntheses of 6H-dibenzo[b,d] pyran-6-one and Its Derivatives
-
Key words:
- 6H-dibenzo[b,d]pyran-6-one
- / C-H bond activation
- / intramolecular cyclization
- / Biphenyl
-
-
[1] H Ishimoto, M Shibata, Y Myojin et al. Bioorg. Med. Chem. Lett., 2011, 21(19):5901~5904.
-
[2] S Cao, C Rossant, S Ng et al. Phytochemistry, 2003, 64(5):987~990.
-
[3] J A Giménez-Bastida, P Truchado, M Larrosa et al. Food Chem., 2012, 132(3):1465~1474.
-
[4] L S Adams, Y J Zhang, D Heber et al. Cancer Prev. Res., 2010, 3(1):108~113.
-
[5] Z Qiu, B Zhou, L Jin et al. Food Chem. Toxicol., 2013, 59:428~437.
-
[6] M Krzeszewski, O Vakuliuk, D T Gryko. Eur. J. Org. Chem., 2013, 2013(25):5631~5644.
-
[7] H G Rule, E Bretscher. J. Chem. Soc., 1927, 925~928.
-
[8] W R H Hurtley. J. Chem. Soc., 1929, 1870~1873.
-
[9] D H Hey, J A Leonard, C W Rees. J. Chem. Soc., 1962, 4579~4584.
-
[10] M J Sharp, V Snieckus. Tetrahed. Lett., 1985, 26(49):5997~6000.
-
[11] B I Alo, A Kandil, P A Patil et al. J. Org. Chem., 1991, 56(12):3763~3768.
-
[12] S Chamoin, S Houldsworth, C G Kruse et al. Tetrahed. Lett., 1998, 39(24):4179~4182.
-
[13] G J Kemperman, B Ter Horst, D van de Goor et al. Eur. J. Org. Chem., 2006, 2006(14):3169~3174.
-
[14] N Thasana, R Worayuthakarn, P Kradanrat et al. J. Org. Chem., 2007, 72(24):9379~9382.
-
[15] J Luo, Y Lu, S Liu et al. Adv. Synth. Catal., 2011, 353(14~15):2604~2608.
-
[16] K L Engelman, Y Feng, I E A son. Organometallics, 2011, 30(17):4572~4577.
-
[17] R Singha, S Roy, S Nandi et al. Tetrahed. Lett., 2013, 54(7):657~660.
-
[18] R S Cahn. J. Chem. Soc., 1933, 1400~1405.
-
[19] R A Heacock, D H Hey. J. Chem. Soc., 1954, 2481~2484.
-
[20] H Togo, T Muraki, M Yokoyama. Tetrahed. Lett., 1995, 36(39):7089~7092.
-
[21] S Luo, F X Luo, X S Zhang et al. Angew. Chem. Int. Ed., 2013, 52(40):10598~10601.
-
[22] K Inamoto, J Kadokawa, Y Kondo. Org. Lett., 2013, 15(15):3962~3965.
-
[23] L Z Huang, R Y Ma, L N Zhou et al. Nat. Product Commun., 2017, 12(4):537~540.
-
[24] J A Teske, A Deiters. Org. Lett., 2008, 10(11):2195~2198.
-
[25] T Kawasaki, Y Yamamoto. J. Org. Chem., 2002, 67(15):5138~5141.
-
[26] I Hussain, V T H Nguyen, M A Yawer et al. J. Org. Chem., 2007, 72(16):6255~6258.
-
[27] M A Terzidis, C A Tsoleridis, J Stephanidou-Stephanatou et al. Tetrahedron, 2008, 64(51):11611~11617.
-
[28] V O Iaroshenko, S A Abbasi Muhammad, A Villinger et al. Tetrahed. Lett., 2011, 52(45):5910~5912.
-
[29] M Khoobi, A Ramazani, A Foroumadi et al. Helv. Chim. Acta, 2013, 96(5):906~918.
-
[30] M E Jung, D A Allen. Org. Lett., 2009, 11(3):757~760.
-
[31] I R Pottie, P R Nandaluru, W L Benoit et al. J. Org. Chem., 2011, 76(21):9015~9030.
-
[32] Y He, X Y Zhang, L G Cui et al. Green Chem., 2012, 14(12):3429~3435.
-
[33] (a)J Barluenga, F J Fañanás, R Sanz et al. Chem. Eur. J., 2002, 8(9):2034~2046; (b) R Sanz, Y Fernández, M P Castroviejo et al. Eur. J. Org. Chem., 2007, 2007(1):62~69.
-
[34] J Zhou, L Z Huang, Y Q Li et al. Tetrahed. Lett., 2012, 53(52):7036~7039.
-
[35] J Zhou, P Han, Y M Xu et al. Heterocycles, 2013, 87(9):1889~1896.
-
-
扫一扫看文章
计量
- PDF下载量: 0
- 文章访问数: 0
- HTML全文浏览量: 0

下载: