Ashburn Bradley O, Carter Rich G, Zakharov Lev N
Department of Chemistry, 153 Gilbert Hall, Oregon State University, Corvallis, Oregon 97331, USA.
J Am Chem Soc. 2007 Jul 25;129(29):9109-16. doi: 10.1021/ja071163r. Epub 2007 Jun 29.
The application of the Diels-Alder approach to biaryls (DAB) is described for the synthesis of tetra-ortho-substituted biaryl compounds containing orthogonally functionalized substituents. The syntheses of phosphorus-containing, disubstituted alkynes and carbonyl-containing, disubstituted alkynes were accomplished in two to three steps from commercially available reagents. Subsequent Diels-Alder cycloadditions with a range of oxygenated dienes yielded the target biaryls. Further functionalization through palladium-couplings is demonstrated on the phosphorus-containing biaryls. In addition, selective manipulation of each of the remaining ortho substituents on the phosphorus-containing biaryls is demonstrated. One of these phosphorus-containing derivatives is utilized as a highly active catalyst for Suzuki coupling. For the carbonyl-containing series, a wide range of dienophile substituents were screened including esters, ketones, and amides. The key Diels-Alder cycloadditions proceeded smoothly with the commercially available 1-methoxy-1,3-cyclohexadiene to yield the resultant tetra-ortho-substituted biaryls with excellent regioselectivity. The scope of the cycloaddition process was also explored on the carbonyl-containing dienophiles with a series of cyclic dienes. Acyclic dienes were also screened; however, they did not prove effective in the Diels-Alder process with the carbonyl-containing acetylenes. The ability to isolate enantiomerically pure biaryl atropisomers using a benzyl oxazolidinone is disclosed. Finally, the subsequent conversion to an axially chiral anilino alcohol is also reported.
描述了双烯加成法用于联芳基化合物(DAB)的应用,以合成含有正交官能化取代基的四邻位取代联芳基化合物。从市售试剂出发,通过两到三步完成了含磷二取代炔烃和含羰基二取代炔烃的合成。随后,与一系列氧化二烯进行双烯加成环化反应,得到目标联芳基化合物。在含磷联芳基化合物上展示了通过钯偶联进行的进一步官能化。此外,还展示了对含磷联芳基化合物上其余每个邻位取代基的选择性操作。其中一种含磷衍生物被用作铃木偶联的高活性催化剂。对于含羰基系列,筛选了多种亲双烯体取代基,包括酯、酮和酰胺。关键的双烯加成环化反应与市售的1-甲氧基-1,3-环己二烯顺利进行,以优异的区域选择性得到所得的四邻位取代联芳基化合物。还研究了含羰基亲双烯体与一系列环状二烯的环化加成反应范围。也筛选了非环状二烯;然而,它们在与含羰基乙炔的双烯加成反应中未证明有效。公开了使用苄基恶唑烷酮分离对映体纯的联芳基阻转异构体的能力。最后,还报道了随后转化为轴向手性苯胺醇的过程。