Monti Chiara, Gennari Cesare, Piarulli Umberto
Dipartimento di Chimica Organica e Industriale, Centro di Eccellenza C.I.S.I. Università degli Studi di Milano, Istituto di Scienze e Tecnologie Molecolari (ISTM) del CNR, 20133 Milano, Italy.
Chemistry. 2007;13(5):1547-58. doi: 10.1002/chem.200600960.
A library of 19 chiral tropos phosphorus ligands, based on a free-to-rotate (tropos) biphenol unit and a chiral P-bonded alcohol (11 phosphites, 1-P(O)(2)O to 11-P(O)(2)O) or secondary amine (8 phosphoramidites, 12-P(O)(2)N to 19-P(O)(2)N), were screened, individually and in combinations of two, in the rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to enones and enoates. High enantioselectivities (up to 99 % ee) and excellent yields were obtained in the addition to either cyclic or acyclic substrates. The flexible biphenolic P ligands outperformed the analogous rigid binaphtholic P ligands. Variable-temperature (31)P NMR studies revealed that the biphenolic ligands are tropos even at low temperature. Only below 190 K was a coalescence observed; upon further cooling, two atropisomers were detected. The Rh homocomplexes (Rh(L(a))(2)) were also studied: in general, a single doublet (P-Rh coupling) was observed in the case of the biphenolic phosphite ligands, over the temperature range 380-230 K, demonstrating their tropos nature in the rhodium complexes even at low temperatures. On the other hand, the phosphoramidites showed different behaviors depending on the structure of the ligand and on the nature of the rhodium source. The spectrum at 230 K of the mixture of [Rh(acac)(eth)(2)] (eth=C(2)H(4)) with phosphite 6-P(O)(2)O and phosphoramidite 19-P(O)(2)N (the most enantioselective ligand combination in the conjugate addition reaction) revealed the presence of four homocomplexes (total approximately 40 %: [Rh{6-P(O)(2)O}(2)], [Rh{(aR)-19-P(O)(2)N}(2)], [Rh{(aS)-19-P(O)(2)N}(2)], [Rh{(aR)-19-P(O)(2)N}{(aS)-19-P(O)(2)N}]) and one heterocomplex, [Rh{6-P(O)(2)O}{(aR)-19-P(O)(2)N}] (approximately 60 %) In the heterocomplex, the biphenol-derived phosphite is free to rotate (tropos) while the biphenol-derived phosphoramidite shows a temperature-dependent tropos/atropos behavior (coalescence temperature=310 K).
基于可自由旋转(扭转)的双酚单元和手性磷键合醇(11种亚磷酸酯,1 - P(O)(2)O至11 - P(O)(2)O)或仲胺(8种亚磷酰胺,12 - P(O)(2)N至19 - P(O)(2)N)构建了一个包含19种手性扭转磷配体的库,并在铑催化的芳基硼酸与烯酮和烯酸酯的不对称共轭加成反应中,对这些配体进行了单独以及两两组合的筛选。在与环状或非环状底物的加成反应中,获得了高对映选择性(高达99% ee)和优异的产率。柔性双酚型磷配体的表现优于类似的刚性联萘酚型磷配体。变温(31)P NMR研究表明,即使在低温下,双酚型配体也是扭转的。仅在190 K以下观察到谱线合并;进一步冷却后,检测到两种阻转异构体。还对铑同配合物(Rh(L(a))(2))进行了研究:一般来说,在380 - 230 K的温度范围内,双酚型亚磷酸酯配体的情况下观察到单一的双峰(P - Rh耦合),这表明它们即使在低温下在铑配合物中也是扭转的。另一方面,亚磷酰胺根据配体结构和铑源的性质表现出不同的行为。[Rh(acac)(eth)(2)](eth = C(2)H(4))与亚磷酸酯6 - P(O)(2)O和亚磷酰胺19 - P(O)(2)N(共轭加成反应中对映选择性最高的配体组合)混合物在230 K时的光谱显示存在四种同配合物(总计约40%:[Rh{6 - P(O)(2)O}(2)]、[Rh{(aR)-19 - P(O)(N}(2)]、[Rh{(aS)-19 - P(O)(2)N}(2)]、[Rh{(aR)-19 - P(O)(2)N}{(aS)-19 - P(O)(2)N}])和一种杂配合物[Rh{6 - P(O)(2)O}{(aR)-19 - P(O)(2)N}](约60%)。在杂配合物中,双酚衍生的亚磷酸酯可自由旋转(扭转),而双酚衍生的亚磷酰胺表现出温度依赖性的扭转/阻转行为(合并温度 = 310 K)。