Allenylphosphonates with a 1,3,2-dioxaphosphorinane ring: Synthesis, structures, stability and utility

被引:40
作者
Bhuvan Kumar N.N. [1 ]
Chakravarty M. [1 ]
Satish Kumar N. [1 ]
Sajna K.V. [1 ]
Kumara Swamy K.C. [1 ]
机构
[1] School of Chemistry, University of Hyderabad
关键词
Allenylphosphonate; Cycloaddition; Horner-Wadsworth-Emmons reaction; Phosphonyl-cyclobutane; X-ray crystal structure;
D O I
10.1007/s12039-009-0003-1
中图分类号
学科分类号
摘要
Synthesis, structures and stability (thermal and air) of allenylphosphonates of the type (OCH2CMe2CH2O)P (O)C (R)=C=CR'R" and [R'R'C=C=C (R)P (O) (OCH2) 2]2C are discussed. Thermally activated dimerization (cycloaddition) of (OCH2CMe2CH2O)P (O)C (H)=C=CMe2 leads to the phosphonocyclobutane [ (OCH 2CMe2CH2O)P (O)C (H)=]2 [C-CMe 2]2 (18). Many of these allenes undergo addition of diefhylamine to lead to enaminophosphonates that are readily hydrolysed by water to lead to β-ketophosphonates. The latter compounds are useful as Horner-Wadsworth-Emmons (HWE) reagents. Molecular structures of (OCH 2CMe2CH2O)P (O)C (CH2OH)=C=CH 2 (6), [H2C=C=C (H)P(O)(OCH2)2] 2C (9). (OCH2CMe2CH2O)P(O)CH=C= CH2 (12), [(OCH2CMe2CH2O)P(O)C(H)=] 2 [C-CMe2]2 (18), and the β- ketophosphonate (OCH2CMe2CH2O)P(O)CH 2)-C(O)CHMe2 (24) have been determined. In compound 6, intermolecular hydrogen bonding between the phosphoryl oxygen and the hydroxyl group leading to an infinite chain is observed. In 6, there is a significant deviation (ca 7°) from the orthogonality expected between the planes containing 4 atoms of (a) H2C=C and (b) C=C(H)P in the allene part. In 9, weak C-H...O interaction between the phosphoryl oxygen atom and a CH 2 proton of the six-membered ring is present. © Indian Academy of Sciences.
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页码:23 / 36
页数:13
相关论文
共 35 条
[1]  
Zimmer R., Dinesh C.U., Nandanan E., Khan F.A., Chem. Rev, 100, (2000)
[2]  
Lu X., Zhang C., Xu Z., Acc. Chem. Res, 34, (2001)
[3]  
Ma S., Chem. Rev, 105, (2005)
[4]  
Hassan H.H.A.M., Current Organic Synthesis, 4, (2007)
[5]  
Brummond K.M., DeForrest J.E., Synthesis, (2006)
[6]  
Nishimura T., Hirabayashi S., Hayashi T., J. Am. Chem. Soc, 126, (2006)
[7]  
Ma S., Guo H., Yu F., J. Org. Chem, 71, (2006)
[8]  
Kumara Swamy K.C., Kumaraswamy S., Senthil Kumar K., Muthiah C., Tetrahedron Lett, 46, (2005)
[9]  
Kommana P., Satish Kumar N., Vittal J.J., Javasree E.G., Jemmis E.D., Kumara Swamy K.C., Org. Lett, 6, (2004)
[10]  
Chakravarty M., Kumara Swamy K.C., J. Org. Chem, 71, (2006)