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源自二十面体邻碳硼烷的B,B'-双(芳基)衍生物的碳环化合物的合成。

The synthesis of carboacycles derived from B,B'-bis(aryl) derivatives of icosahedral ortho-carborane.

作者信息

Bayer Michael J, Herzog Axel, Diaz Martin, Harakas George A, Lee Hans, Knobler Carolyn B, Hawthorne M Frederick

机构信息

Department of Chemistry and Biochemistry, University of California, Los Angeles, 90095, USA.

出版信息

Chemistry. 2003 Jun 16;9(12):2732-44. doi: 10.1002/chem.200304803.

Abstract

Reactions of both closo-9,12-I2-1,2-C2B10H10 and closo-9,10-I2-1,7-C2B10H10 with an excess of aryl magnesium bromide in the presence of [PdCl2(PPh3)2] afford the corresponding closo-9,12-(4-R-C6H4)2-1,2-C2B10H10 [R=H (1), Me (2), OMe (3), SMe (4), N(CH3)2 (5), Cl (6)] and closo-9,10-(4-R-C6H4)2-1,7-C2B10H10 [R'=Me (7), OMe (8), N(CH3)2 (9), Cl (10), and -C[(OCH2)2]CH3 (11)] compounds in high yields. The anisole derivatives 3 and 8 were deprotected to yield the corresponding bis-phenols 12 and 13, respectively. Structural analyses of compounds 1, 3, 6, and 12 are reported. Re-etherification of compound 12 by using gamma-bromotriethyleneglycol methyl ether provided 14 (R=(CH2CH2O)3CH3). Oxidation of 4 with ceric(IV) ammonium nitrate (CAN) generated the bis-sulfoxide 15 (R=S(O)Me). Deprotection of compound 11 led to the corresponding acetyl derivative 18 (R'=C(O)Me). Bis-anisole 3 was tethered with 1,3-dibromopropane, 1,6-dibromohexane, 1,8-dibromooctane, 4,4'-bis(iodomethyl)-1,1'-biphenyl, and alpha,alpha'-dibromo-2,6-lutidine to afford the dimers 20b, 21b, 22b, 23b, and 24b, respectively. The tetrameric carboracycles 27a and 30a, as well as the dimeric 29c were obtained through repetitive coupling of the dimeric compounds 20b, 24b, and 22b with 1,3-dibromopropane, alpha,alpha'-dibromo-2,6-lutidine, and 1,8-dibromooctane, respectively. The tetrameric carboracycle 28a was obtained upon consecutive reactions of 1 with 1,4-dibromobutane. Hexameric carboracycle 28b was identified as a byproduct. Exhaustive ether cleavage of 27a generated octaphenol 31a. Re-etherification of 31a with trimethylenesultone provided the octasulfonate 32a, the first example of a water-soluble carboracycle. Linkage of dimer 23b with alpha,alpha'-dibromolutidine yielded the cyclic tetrameric tetrapyridyl derivative 30a in low yield. The structures of the carboracycles 27a, 28a, 28b, and 30a have been confirmed by Xray crystallography. In addition, the compounds 28a,b are the first reported carboracycles that interact with solvent molecules in a host-guest fashion.

摘要

在[PdCl₂(PPh₃)₂]存在下,笼型-9,12-二碘-1,2-碳硼烷(closo-9,12-I₂-1,2-C₂B₁₀H₁₀)和笼型-9,10-二碘-1,7-碳硼烷(closo-9,10-I₂-1,7-C₂B₁₀H₁₀)与过量的芳基溴化镁反应,高产率地得到相应的笼型-9,12-(4-R-苯基)₂-1,2-碳硼烷[R = H (1)、甲基 (2)、甲氧基 (3)、甲硫基 (4)、N(CH₃)₂ (5)、氯 (6)]和笼型-9,10-(4-R-苯基)₂-1,7-碳硼烷[R' = 甲基 (7)、甲氧基 (8)、N(CH₃)₂ (9)、氯 (10)和 -C[(OCH₂)₂]CH₃ (11)]化合物。茴香醚衍生物3和8脱保护后分别得到相应的双酚12和13。报道了化合物1、3、6和12的结构分析。用γ-溴代三乙二醇甲醚对化合物12进行再醚化反应得到14(R = (CH₂CH₂O)₃CH₃)。用硝酸铈铵(CAN)氧化4生成双亚砜15(R = S(O)Me)。化合物11脱保护得到相应的乙酰基衍生物18(R' = C(O)Me)。双茴香醚3与1,3-二溴丙烷、1,6-二溴己烷、1,8-二溴辛烷、4,4'-双(碘甲基)-1,1'-联苯和α,α'-二溴-2,6-二甲基吡啶反应,分别得到二聚体20b、21b、22b、23b和24b。通过二聚体化合物20b、24b和22b分别与1,3-二溴丙烷、α,α'-二溴-2,6-二甲基吡啶和1,8-二溴辛烷重复偶联反应,得到四聚碳硼烷27a和30a以及二聚体29c。1与1,4-二溴丁烷连续反应得到四聚碳硼烷28a。六聚碳硼烷28b被鉴定为副产物。27a进行彻底的醚键裂解得到八酚31a。31a用三亚甲基环丁砜进行再醚化反应得到八磺酸酯32a,这是水溶性碳硼烷的首例。二聚体23b与α,α'-二溴-2,6-二甲基吡啶连接,低产率地得到环状四聚四吡啶基衍生物30a。碳硼烷2综合利用27a、28a、28b和30a的结构已通过X射线晶体学确证。此外,化合物28a、b是首次报道的以主客体方式与溶剂分子相互作用的碳硼烷。

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