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Effect of amino substituents on the stereochemical outcome of the photo-Arbuzov rearrangements of 1-arylethyl phosphorodiamidites

机译:氨基取代基对1-芳基乙基亚磷酰胺的光-Arbuzov重排的立体化学结果的影响

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The essentially stereochemically pure 1-arylethyl phosphorodiamidites 8 and 9 were irradiated by UV light in acetonitrile, benzene, and cyclohexane (Tables 1-4). Reaction via singlet free-radical pairs, formed by carbon-oxygen bond scission (Scheme 1), which are somewhat longer lived than those from the analogous phosphites 5 and 6, is proposed. Tetramethyl 1-phenylethylphosphorodiamidite (8) gives the photo-Arbuzov rearrangement product 10 in 59% +/- 2% GC yield, based on percent 8 consumed (Tables 1 and 4), along with the free radical dimerization product 2,3-diphenylbutane, 12a, in in amounts corresponding to ca. 19% of the potentially formed 1-phenylethyl radicals. Similarly, from 9, the photorearrangement product 11 is generated in 64 +/- 4% yield (Tables 2 and 4) along with a 18 +/- 2% accountability of the 1-naphthylethyl radicals as 12b. The photorearrangement of stereochemically enriched 8 (RIS = 99:1) gives 10 in which an apparent 67 +/- 2% (100y, eq 3, Table 4) of the initial radical pairs [3,14] recombine with retention of configuration at the stereogenic carbon (34 +/- 3% net retention, eq 5). With TEMPO present, 70% (100y, eq 3) of the initial 1-phenylethyl radicals, 14, from 8 combine with radicals 3 in the solvent cage with retained configuration at carbon (40% percent net retention, eq 5). The yield of product 10 is reduced to 54%, and 12a is absent. Similarly, the five-membered ring naphthylethyl analogue, phosphorodiamidite 9 (RIS = 98:2), affords largely (R)-11 with apparent 34 +/- 3% net retention. The degree of stereorandomization observed in these systems is higher than was reported previously for phosphites 5 and 6. The neglect of reconversion of pro-S 14 to pro-R 14 on the results of these studies is addressed. Estimated maximum values (eq 4) of k(comb)/k(rot) (2.3) for the proximate radical pairs [3,14] from 8 with TEMPO present appear to be at least 6-fold smaller than those of the analogous phosphite (R)-5 (average k(comb)/k(rot) = 13 with TEMPO present). Possible origins for this effect are proposed.
机译:用UV光在乙腈,苯和环己烷中辐照基本上立体化学纯的1-芳基乙二磷酰胺8和9(表1-4)。提出了通过碳-氧键断裂形成的单线自由基对的反应(方案1),其寿命比类似亚磷酸酯5和6更长。基于消耗的8%(表1和表4),四甲基1-苯基乙基亚磷酰胺基二(8)以59%+/- 2%的GC收率得到光-Arbuzov重排产物10,以及自由基二聚产物2,3-二苯基丁烷,约12a,其量对应于约。 19%的潜在形成的1-苯基乙基基团。类似地,从9开始,以64 +/- 4%的收率(表2和4)生成光重排产物11,以及18 +/- 2%的1-萘乙基自由基作为12b。立体化学富集的8(RIS = 99:1)的光重排得到10,其中初始自由基对[3,14]的表观67 +/- 2%(100y,eq 3,表4)重组并保留构型为立体碳(34 +/- 3%的净保留,当量5)。在存在TEMPO的情况下,最初的1-苯基乙基自由基(14个中的8个)中有70%(100y,当量3)与自由基3结合在溶剂笼中,并在碳上保留了构型(净保留率为40%,当量5)。产品10的产率降低到54%,并且不存在12a。类似地,五元环萘基乙基类似物亚磷酰胺基二磷酸酯9(RIS = 98:2)可以提供大量的(R)-11,其净保留率为34 +/- 3%。在这些系统中观察到的立体随机化程度高于先前对亚磷酸酯5和6的报道。解决了这些研究结果对前S 14向前R 14转化的忽视。来自存在TEMPO的8个基团对[3,14]的k(comb)/ k(rot)(2.3)的估计最大值(eq 4)至少比类似亚磷酸酯小6倍(R)-5(在有TEMPO的情况下,平均k(comb)/ k(rot)= 13)。提出了这种效果的可能来源。

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