[1] | Brown C,Farthing A.Preparation and Structure of Di-p-xylylene[J]. Nature,1949,164(4178):915-916. | [2] | Aly A A,Brown A B.Asymmetric and Fused Heterocycles Based on [2.2] Paracyclophane[J]. Tetrahedron,2009,39(65):8055-8089. | [3] | Miyazaki T,Shibahara M,Fujishige J I,et al. Synthesis and Electronic and Photophysical Properties of [2.2]- and [3.3] Paracyclophane-Based Donor-Donor'-Acceptor Triads[J]. J Org Chem,2014,79(23):11440-11453. | [4] | Gibson S E,Knight J D.[2.2] Paracyclophane Derivatives in Asymmetric Catalysis[J]. Org Biomol Chem,2003,1(8):1256-1269. | [5] | Yeh Y L,Gorham W F.Preparation and Reactions of Some [2.2] Paracyclophane Derivatives[J]. J Org Chem,1969,34(8):2366-2370. | [6] | Wynberg H.The Reimer-Tiemann Reaction[J]. Chem Rev,1960,60(2):169-184. | [7] | Paradies J.[2.2] Paracyclophane Derivatives:Synthesis and Application in Catalysis[J]. Synthesis,2011,(23):3749-3766. | [8] | David O R.Syntheses and Applications of Disubstituted [2.2] Paracyclophanes[J]. Tetrahedron,2012,44(68):8977-8993. | [9] | Braun C,Bräse S,Schafer L L.Planar-Chiral [2.2] Paracyclophane-Based Amides as Proligands for Titanium and Zirconium-Catalyzed Hydroamination[J]. Eur J Org Chem,2017,(13):1760-1764. | [10] | Delcourt M L,Turcaud S,Benedetti E,et al. Efficient and Scalable Kinetic Resolution of Racemic 4-Formyl [2.2] Paracyclophane via Asymmetric Transfer Hydrogenation[J]. Adv Synth Catal,2016,358(8):1213-1218. | [11] | Cakici M,Gu Z G,Nieger M,et al. Planar-Chiral Building Blocks for Metal-Organic Frameworks[J]. Chem Commun,2015,51(23):4796-4798. | [12] | Friedmann C J,Ay S, Brase S.Improved Synthesis of Enantiopure 4-Hydroxy [2.2] Paracyclophane[J]. J Org Chem,2010,75(13):4612-4614. |
|