高等学校化学学报 ›› 2020, Vol. 41 ›› Issue (10): 2256.doi: 10.7503/cjcu20200307
收稿日期:
2020-05-29
出版日期:
2020-10-10
发布日期:
2020-10-08
通讯作者:
汤卫军
E-mail:tangwj@snnu.edu.cn
基金资助:
WANG Biwen1,2, DU Tian1, TANG Weijun1()
Received:
2020-05-29
Online:
2020-10-10
Published:
2020-10-08
Contact:
TANG Weijun
E-mail:tangwj@snnu.edu.cn
Supported by:
摘要:
设计并合成了一系列基于(R)-2-(二苯基膦基)-1-苯基-N-(2′-吡啶甲基)-1-乙胺及其衍生物的手性钌螯合催化剂. 采用核磁共振波谱及高分辨质谱对其进行表征, 并给出单晶结构. 以α-羟基酯类化合物为研究对象, 通过酯的动态动力学氢化还原反应, 发展了一种合成手性二醇的方法.研究结果表明, 该催化体系能有效实现酯的氢化还原, 并获得一定的对映选择性.
中图分类号:
TrendMD:
汪贲文, 杜甜, 汤卫军. 手性钌螯合催化剂的合成及在α⁃羟基酯的动态动力学氢化反应中的应用. 高等学校化学学报, 2020, 41(10): 2256.
WANG Biwen, DU Tian, TANG Weijun. Synthesis and Application of Chiral Ru Pincer Catalysts on the Hydrogenation of α-Hydroxy Esters by Dynamic Kinetic Resolution†. Chem. J. Chinese Universities, 2020, 41(10): 2256.
Compd. | Appearance | Yields(%) | HRMS(calcd.), m/z [M-Cl]+ |
---|---|---|---|
Cat.1 | Yellow solid | 56 | 795.1393(795.1366) |
Cat.2 | Yellow solid | 57 | 873.0498(873.0456) |
Cat.3 | Yellow solid | 50 | 809.1550(809.1516) |
Cat.4 | Yellow solid | 50 | 825.1499(825.1453) |
Cat.5 | Yellow solid | 62 | 853.1812(853.1754) |
Cat.6 | Yellow solid | 71 | 871.1706(871.1673) |
Cat.7 | Yellow solid | 68 | 878.2128(878.2077) |
Cat.8 | Yellow solid | 51 | 892.2285(892.2214) |
Cat.9 | Yellow solid | 68 | 873.0498(873.0396) |
Cat.10 | Yellow solid | 69 | 887.0655(887.0558) |
Cat.11 | Yellow solid | 53 | 809.1550(809.1380) |
Cat.12 | Brown solid | 48 | 845.1550(845.1485) |
Table 1 Appearance, yields and HRMS data of compounds Cat.1—Cat.12
Compd. | Appearance | Yields(%) | HRMS(calcd.), m/z [M-Cl]+ |
---|---|---|---|
Cat.1 | Yellow solid | 56 | 795.1393(795.1366) |
Cat.2 | Yellow solid | 57 | 873.0498(873.0456) |
Cat.3 | Yellow solid | 50 | 809.1550(809.1516) |
Cat.4 | Yellow solid | 50 | 825.1499(825.1453) |
Cat.5 | Yellow solid | 62 | 853.1812(853.1754) |
Cat.6 | Yellow solid | 71 | 871.1706(871.1673) |
Cat.7 | Yellow solid | 68 | 878.2128(878.2077) |
Cat.8 | Yellow solid | 51 | 892.2285(892.2214) |
Cat.9 | Yellow solid | 68 | 873.0498(873.0396) |
Cat.10 | Yellow solid | 69 | 887.0655(887.0558) |
Cat.11 | Yellow solid | 53 | 809.1550(809.1380) |
Cat.12 | Brown solid | 48 | 845.1550(845.1485) |
Compd. | 1H NMR(400MHz, CDCl3), δ | 13C NMR(100MHz, CDCl3), δ | 31P NMR(162 MHz, CDCl3), δ |
---|---|---|---|
Cat.1 | 8.48(s, 1H), 7.77(t, J=8.6 Hz, 2H), 7.52—7.07(m, 30H), 6.83—6.80(m, 1H), 5.63—5.57(m, 1H), 5.41—5.34(m, 1H), 4.83—4.78(m, 1H), 3.76—3.73(m, 1H), 3.40—3.32(m, 1H), 2.93—2.87(m, 1H) | 162.8, 156.3, 139.0, 134.9, 134.7, 134.0(d, J=9.1 Hz), 129.2, 128.9, 128.7, 128.6, 127.4, 127.3, 127.2, 127.1, 127.0, 122.5, 121.5, 64.0(d, J=6.3 Hz), 55.0, 46.4(d, J=25.7 Hz) | 47.8(d, J=30.0 Hz,1P), 37.6(d, J=31.4 Hz, 1P) |
Cat.2 | 8.28(brs, 1H), 7.64—7.08(m, 21H), 7.00—6.95(m, 10H), 6.53—6.49(m, 1H), 5.53—5.47(m, 1H), 5.13—5.06(m, 1H), 4.73—4.66(m, 1H), 4.09—4.03(m, 1H), 3.27—3.19(m, 1H), 2.81—2.74(m, 1H) | 161.4, 155.2, 139.8, 135.1(d, J=15.2 Hz), 136.9, 136.6, 135.1, 135.0, 134.9, 134.0(d, J=9.1 Hz), 127.3(d, J=9.3 Hz), 129.3, 129.1, 128.8, 128.7, 127.4, 127.3, 127.2, 127.1, 126.8, 123.0, 117.8, 64.2(d, J=5.2 Hz), 53.5, 46.5(d, J=26.1 Hz) | 47.1(d, J=31.2 Hz,1P), 38.3(d, J=31.9 Hz, 1P) |
Cat.3 | 8.19(brs, 1H), 7.67—7.50(m, 10H), 7.45—6.96(m, 22H), 5.62—5.55(m, 1H), 5.28—5.22(m, 1H), 4.84—4.75(m, 1H), 3.72—3.66(m, 2H), 3.45—3.26(m, 1H), 2.99—2.92(m, 1H), 1.86(s, 1H) | 159.6, 156.8, 139.1(d, J=15.5 Hz), 137.8, 137.5, 137.1, 136.7(d, J=3.3 Hz), 135.1(d, J=9.7 Hz), 134.8(d, J=8.5 Hz), 134.1(d, J=9.2 Hz), 132.3, 129.2, 128.9, 128.7(d, J=1.3 Hz), 128.5, 127.4, 127.3, 127.2, 127.1, 127.0, 120.7, 64.1(d, J=5.9 Hz), 54.8, 46.6(d, J=25.8 Hz), 18.12 | 47.7(d, J=31.2 Hz,1P), 38.4(d, J=30.9 Hz, 1P) |
Cat.4 | 8.29(brs, 1H), 7.73—7.68(m, 2H), 7.50—6.96(m, 30H), 5.61—5.55(m, 1H), 5.25—5.18(m, 1H), 4.80—4.72(m, 1H), 3.69—3.63(m, 2H), 3.33—3.22(m, 1H), 3.26(s, 1H), 2.87—2.81(m, 1H) | 155.0, 154.2(d, J=3.2 Hz), 142.7(d, J=2.5 Hz), 139.1, 139.0, 137.6, 137.1, 136.7, 135.1, 135.0, 134.9, 134.1(d, J=9.2 Hz), 129.2, 129.0, 128.8, 128.6, 127.3(d, J=8.8 Hz), 127.1(d, J=9.2 Hz), 127.0, 123.6, 121.6, 63.8(d, J=5.7 Hz), 54.4, 53.5, 46.4(d, J=26.1 Hz) | 48.1(d, J=30.5 Hz,1P), 37.5(d, J=30.5 Hz, 1P) |
Cat.5 | 8.25(s, 1H), 7.71(t, J=8.6 Hz, 2H), 7.52—7.01(m, 30H), 5.61—5.55(m, 1H), 5.32—5.23(m, 1H), 4.84—4.77(m, 1H), 3.74—3.65(m, 2H), 3.56—3.28(m, 1H), 2.92—2.85(m, 1H), 1.07—1.04(m, 6H) | 155.9, 154.2, 145.9, 140.5(d, J=15.2 Hz), 139.1, 138.8, 138.5, 138.1, 136.5(d, J=9.7 Hz), 136.3(d, J=8.6 Hz), 135.6(d, J=9.2 Hz), 130.6, 130.1, 129.9, 128.7(d, J=8.7 Hz), 126.4, 123.2, 72.1, 65.3(d, J=5.5 Hz), 55.8, 47.8(d, J=26.2 Hz), 23.3, 22.8 | 48.0(d, J=30.0 Hz,1P), 37.6(d, J=30.0 Hz, 1P) |
Cat.6 | 8.86(s, 1H), 7.74—7.67(m, 3H), 7.50—7.02(m, 32H), 6.91—6.89(m, 2H), 5.67—5.61(m, 1H), 5.37—5.34(m, 1H), 4.82—4.75(m, 1H), 3.77—3.72(m, 1H), 3.35—3.27(m, 1H), 2.89—2.83(m, 1H) | 161.2, 155.2, 139.1, 138.9, 137.7, 137.3, 137.1, 136.7, 136.3, 135.8, 135.0(d, J=9.5 Hz), 134.4, 134.1(d, J=9.2 Hz), 129.2, 129.0, 128.8, 128.7, 128.6, 128.2, 127.4, 127.3, 127.2, 127.1, 127.0, 126.9, 121.5, 64.0(d, J=5.5 Hz), 53.4, 46.4(d, J=25.0 Hz) | 48.1(d, J=30.6 Hz,1P), 37.3(d, J=29.7 Hz, 1P) |
Compd. | 1H NMR(400MHz, CDCl3), δ | 13C NMR(100MHz, CDCl3), δ | 31P NMR(162 MHz, CDCl3), δ |
Cat.7 | 8.34(s, 1H), 7.76(t, J=8.6 Hz, 2H), 7.52—6.94(m, 30H), 5.62—5.59(m, 1H), 5.24—5.17(m, 1H), 4.81—4.74(m, 1H), 3.67—3.62(m, 1H), 3.37—3.62(m, 1H), 2.88—2.82(m, 1H), 2.75—2.72(m, 2H), 2.63—2.60(m, 2H), 1.45(s, 6H) | 161.3, 157.2, 138.8, 137.8, 136.6, 136.3, 135.0(d, J=9.6 Hz), 134.5(d, J=8.6 Hz), 133.9(d, J=9.2 Hz), 129.0, 127.4(d, J=8.9 Hz), 127.2(d, J=2.6 Hz), 127.1(d, J=2.0 Hz), 126.8, 122.1, 118.3(d, J=4.5 Hz), 60.6(d, J=3.8 Hz), 54.3, 43.2(d, J=27.8 Hz), 39.5(d, J=15.0 Hz) | 48.2(d, J=29.7 Hz,1P), 37.0(d, J=29.7 Hz, 1P) |
Cat.8 | 8.18—8.16(m, 1H), 7.80—7.76(m, 2H), 7.49—7.00(m, 28H), 6.91—6.89(m, 1H), 6.77—6.74(m, 1H), 5.58—5.52(m, 1H), 5.22—5.16(m, 1H), 4.77—4.68(m, 1H), 3.62—3.56(m, 1H), 3.36—3.28(m, 1H), 2.96—2.86(m, 4H), 2.80—2.73(m, 1H), 1.44—1.26(m, 8H) | 147.3, 142.8, 140.7(d, J=2.8 Hz), 138.3(d, J=15.4 Hz), 136.4, 136.0, 134.1, 134.0, 133.1(d, J=9.1 Hz), 128.1, 127.8(d, J=3.5 Hz), 127.5, 127.3, 126.2(d, J=8.8 Hz), 126.0, 125.9, 120.4, 116.8, 62.5(d, J=5.7 Hz), 53.2, 47.5, 45.3, 45.1, 26.0(d, J=29.5 Hz) | 48.2(d, J=29.5 Hz,1P), 36.7(d, J=29.4 Hz, 1P) |
Cat.9 | 8.40(s, 1H), 7.67—7.60(m, 3H), 7.56—7.20(m, 18H), 7.15—6.97(m, 10H), 5.61—5.56(m, 1H), 5.29—5.23(m, 1H), 4.83—4.76(m, 1H), 3.73—3.67(m, 1H), 3.35—3.67(m, 1H), 3.00—2.93(m, 1H) | 161.4, 157.2, 138.9, 136.7, 136.3, 135.1(d, J=9.8 Hz), 134.84(d, J=8.6 Hz), 134.1(d, J=9.2 Hz), 129.4, 129.1, 129.0, 128.8, 127.5(d, J=9.1 Hz), 127.3(d, J=9.3 Hz), 127.0, 122.1, 118.3, 64.2(d, J=5.2 Hz), 54.7, 46.6(d, J=26.0 Hz) | 47.1(d, J=31.6 Hz,1P), 38.8(d, J=32.2 Hz, 1P) |
Cat.10 | 8.43(s, 1H), 7.69—7.66(m, 1H), 7.51(t, J=4.3Hz, 1H), 7.32—7.23(m, 10H), 7.17—7.01(m, 15H), 5.41—5.35(m, 1H), 5.08—5.02(m, 1H), 4.44—4.40(m, 1H), 4.12—4.10(m, 1H), 3.63—3.60(m, 1H), 2.83—2.77(m, 1H), 2.71—2.68(m, 1H) | 161.3, 157.2, 138.8, 137.8, 136.6, 136.2, 135.0, 134.5(d, J=8.6 Hz), 133.9(d, J=9.2 Hz), 128.9, 128.8, 127.4, 127.3, 127.2(d, J=2.5 Hz), 127.1(d, J=1.9 Hz), 126.8, 122.1, 118.3(d, J=4.4 Hz), 60.6(d, J=4.6 Hz), 54.3, 43.2(d, J=28.3 Hz), 39.5(d, J=15.8 Hz) | 47.2(d, J=32.2 Hz,1P), 38.1(d, J=32.2 Hz, 1P) |
Cat.11 | 8.21—8.16(m, 2H), 7.55—6.68(m, 31H), 5.86—5.79(m, 1H), 5.41—5.34(m, 1H), 5.74—5.71(m, 1H), 4.56—4.52(m, 1H), 3.91—3.87(m, 1H), 3.78—3.70(m, 1H), 2.57—2.52(m, 1H), 2.45(m, 3H) | 165.2, 162.8, 139.1(d, J=16.4 Hz), 138.2, 137.8, 136.7, 135.7(d, J=8.9 Hz), 134.5(d, J=7.9 Hz), 129.3, 129.1, 128.7, 127.2(d, J=8.9 Hz), 127.0, 123.5, 119.4, 63.9(d, J=6.2 Hz), 56.5, 46.4(d, J=28.7 Hz), 29.4 | 43.4(d, J=33.9 Hz,1P), 37.3(d, J=34.8Hz, 1P) |
Cat.12 | 8.47—8.45(m, 1H), 7.88—7.84(m, 2H), 7.75—7.73(m, 2H), 7.66—7.62(m, 1H), 7.58—7.56(m, 2H), 7.52—7.07(m, 28H), 5.83—5.77(m, 1H), 5.63—5.56(m, 1H), 5.00—4.92(m, 1H), 4.63—4.57(m, 1H), 3.48—3.40(m, 1H), 2.96—2.89(m, 1H) | 163.4, 148.2, 139.0, 138.8, 138.0, 137.7, 136.9, 135.1(d, J=9.9 Hz), 134.0(d, J=9.1 Hz), 130.8, 129.3, 129.0(d, J=5.8 Hz), 128.7, 127.9, 127.4, 127.3, 127.2, 127.1, 126.2(d, J=2.0 Hz), 125.0, 119.8, 64.3(d, J=5.9 Hz), 52.4, 46.8(d, J=26.0 Hz) | 47.7(d, J=30.0 Hz,1P), 37.2(d, J=30.9 Hz, 1P) |
Table 2 1H NMR, 13C NMR and 31P NMR data of compounds Cat.1—Cat.12
Compd. | 1H NMR(400MHz, CDCl3), δ | 13C NMR(100MHz, CDCl3), δ | 31P NMR(162 MHz, CDCl3), δ |
---|---|---|---|
Cat.1 | 8.48(s, 1H), 7.77(t, J=8.6 Hz, 2H), 7.52—7.07(m, 30H), 6.83—6.80(m, 1H), 5.63—5.57(m, 1H), 5.41—5.34(m, 1H), 4.83—4.78(m, 1H), 3.76—3.73(m, 1H), 3.40—3.32(m, 1H), 2.93—2.87(m, 1H) | 162.8, 156.3, 139.0, 134.9, 134.7, 134.0(d, J=9.1 Hz), 129.2, 128.9, 128.7, 128.6, 127.4, 127.3, 127.2, 127.1, 127.0, 122.5, 121.5, 64.0(d, J=6.3 Hz), 55.0, 46.4(d, J=25.7 Hz) | 47.8(d, J=30.0 Hz,1P), 37.6(d, J=31.4 Hz, 1P) |
Cat.2 | 8.28(brs, 1H), 7.64—7.08(m, 21H), 7.00—6.95(m, 10H), 6.53—6.49(m, 1H), 5.53—5.47(m, 1H), 5.13—5.06(m, 1H), 4.73—4.66(m, 1H), 4.09—4.03(m, 1H), 3.27—3.19(m, 1H), 2.81—2.74(m, 1H) | 161.4, 155.2, 139.8, 135.1(d, J=15.2 Hz), 136.9, 136.6, 135.1, 135.0, 134.9, 134.0(d, J=9.1 Hz), 127.3(d, J=9.3 Hz), 129.3, 129.1, 128.8, 128.7, 127.4, 127.3, 127.2, 127.1, 126.8, 123.0, 117.8, 64.2(d, J=5.2 Hz), 53.5, 46.5(d, J=26.1 Hz) | 47.1(d, J=31.2 Hz,1P), 38.3(d, J=31.9 Hz, 1P) |
Cat.3 | 8.19(brs, 1H), 7.67—7.50(m, 10H), 7.45—6.96(m, 22H), 5.62—5.55(m, 1H), 5.28—5.22(m, 1H), 4.84—4.75(m, 1H), 3.72—3.66(m, 2H), 3.45—3.26(m, 1H), 2.99—2.92(m, 1H), 1.86(s, 1H) | 159.6, 156.8, 139.1(d, J=15.5 Hz), 137.8, 137.5, 137.1, 136.7(d, J=3.3 Hz), 135.1(d, J=9.7 Hz), 134.8(d, J=8.5 Hz), 134.1(d, J=9.2 Hz), 132.3, 129.2, 128.9, 128.7(d, J=1.3 Hz), 128.5, 127.4, 127.3, 127.2, 127.1, 127.0, 120.7, 64.1(d, J=5.9 Hz), 54.8, 46.6(d, J=25.8 Hz), 18.12 | 47.7(d, J=31.2 Hz,1P), 38.4(d, J=30.9 Hz, 1P) |
Cat.4 | 8.29(brs, 1H), 7.73—7.68(m, 2H), 7.50—6.96(m, 30H), 5.61—5.55(m, 1H), 5.25—5.18(m, 1H), 4.80—4.72(m, 1H), 3.69—3.63(m, 2H), 3.33—3.22(m, 1H), 3.26(s, 1H), 2.87—2.81(m, 1H) | 155.0, 154.2(d, J=3.2 Hz), 142.7(d, J=2.5 Hz), 139.1, 139.0, 137.6, 137.1, 136.7, 135.1, 135.0, 134.9, 134.1(d, J=9.2 Hz), 129.2, 129.0, 128.8, 128.6, 127.3(d, J=8.8 Hz), 127.1(d, J=9.2 Hz), 127.0, 123.6, 121.6, 63.8(d, J=5.7 Hz), 54.4, 53.5, 46.4(d, J=26.1 Hz) | 48.1(d, J=30.5 Hz,1P), 37.5(d, J=30.5 Hz, 1P) |
Cat.5 | 8.25(s, 1H), 7.71(t, J=8.6 Hz, 2H), 7.52—7.01(m, 30H), 5.61—5.55(m, 1H), 5.32—5.23(m, 1H), 4.84—4.77(m, 1H), 3.74—3.65(m, 2H), 3.56—3.28(m, 1H), 2.92—2.85(m, 1H), 1.07—1.04(m, 6H) | 155.9, 154.2, 145.9, 140.5(d, J=15.2 Hz), 139.1, 138.8, 138.5, 138.1, 136.5(d, J=9.7 Hz), 136.3(d, J=8.6 Hz), 135.6(d, J=9.2 Hz), 130.6, 130.1, 129.9, 128.7(d, J=8.7 Hz), 126.4, 123.2, 72.1, 65.3(d, J=5.5 Hz), 55.8, 47.8(d, J=26.2 Hz), 23.3, 22.8 | 48.0(d, J=30.0 Hz,1P), 37.6(d, J=30.0 Hz, 1P) |
Cat.6 | 8.86(s, 1H), 7.74—7.67(m, 3H), 7.50—7.02(m, 32H), 6.91—6.89(m, 2H), 5.67—5.61(m, 1H), 5.37—5.34(m, 1H), 4.82—4.75(m, 1H), 3.77—3.72(m, 1H), 3.35—3.27(m, 1H), 2.89—2.83(m, 1H) | 161.2, 155.2, 139.1, 138.9, 137.7, 137.3, 137.1, 136.7, 136.3, 135.8, 135.0(d, J=9.5 Hz), 134.4, 134.1(d, J=9.2 Hz), 129.2, 129.0, 128.8, 128.7, 128.6, 128.2, 127.4, 127.3, 127.2, 127.1, 127.0, 126.9, 121.5, 64.0(d, J=5.5 Hz), 53.4, 46.4(d, J=25.0 Hz) | 48.1(d, J=30.6 Hz,1P), 37.3(d, J=29.7 Hz, 1P) |
Compd. | 1H NMR(400MHz, CDCl3), δ | 13C NMR(100MHz, CDCl3), δ | 31P NMR(162 MHz, CDCl3), δ |
Cat.7 | 8.34(s, 1H), 7.76(t, J=8.6 Hz, 2H), 7.52—6.94(m, 30H), 5.62—5.59(m, 1H), 5.24—5.17(m, 1H), 4.81—4.74(m, 1H), 3.67—3.62(m, 1H), 3.37—3.62(m, 1H), 2.88—2.82(m, 1H), 2.75—2.72(m, 2H), 2.63—2.60(m, 2H), 1.45(s, 6H) | 161.3, 157.2, 138.8, 137.8, 136.6, 136.3, 135.0(d, J=9.6 Hz), 134.5(d, J=8.6 Hz), 133.9(d, J=9.2 Hz), 129.0, 127.4(d, J=8.9 Hz), 127.2(d, J=2.6 Hz), 127.1(d, J=2.0 Hz), 126.8, 122.1, 118.3(d, J=4.5 Hz), 60.6(d, J=3.8 Hz), 54.3, 43.2(d, J=27.8 Hz), 39.5(d, J=15.0 Hz) | 48.2(d, J=29.7 Hz,1P), 37.0(d, J=29.7 Hz, 1P) |
Cat.8 | 8.18—8.16(m, 1H), 7.80—7.76(m, 2H), 7.49—7.00(m, 28H), 6.91—6.89(m, 1H), 6.77—6.74(m, 1H), 5.58—5.52(m, 1H), 5.22—5.16(m, 1H), 4.77—4.68(m, 1H), 3.62—3.56(m, 1H), 3.36—3.28(m, 1H), 2.96—2.86(m, 4H), 2.80—2.73(m, 1H), 1.44—1.26(m, 8H) | 147.3, 142.8, 140.7(d, J=2.8 Hz), 138.3(d, J=15.4 Hz), 136.4, 136.0, 134.1, 134.0, 133.1(d, J=9.1 Hz), 128.1, 127.8(d, J=3.5 Hz), 127.5, 127.3, 126.2(d, J=8.8 Hz), 126.0, 125.9, 120.4, 116.8, 62.5(d, J=5.7 Hz), 53.2, 47.5, 45.3, 45.1, 26.0(d, J=29.5 Hz) | 48.2(d, J=29.5 Hz,1P), 36.7(d, J=29.4 Hz, 1P) |
Cat.9 | 8.40(s, 1H), 7.67—7.60(m, 3H), 7.56—7.20(m, 18H), 7.15—6.97(m, 10H), 5.61—5.56(m, 1H), 5.29—5.23(m, 1H), 4.83—4.76(m, 1H), 3.73—3.67(m, 1H), 3.35—3.67(m, 1H), 3.00—2.93(m, 1H) | 161.4, 157.2, 138.9, 136.7, 136.3, 135.1(d, J=9.8 Hz), 134.84(d, J=8.6 Hz), 134.1(d, J=9.2 Hz), 129.4, 129.1, 129.0, 128.8, 127.5(d, J=9.1 Hz), 127.3(d, J=9.3 Hz), 127.0, 122.1, 118.3, 64.2(d, J=5.2 Hz), 54.7, 46.6(d, J=26.0 Hz) | 47.1(d, J=31.6 Hz,1P), 38.8(d, J=32.2 Hz, 1P) |
Cat.10 | 8.43(s, 1H), 7.69—7.66(m, 1H), 7.51(t, J=4.3Hz, 1H), 7.32—7.23(m, 10H), 7.17—7.01(m, 15H), 5.41—5.35(m, 1H), 5.08—5.02(m, 1H), 4.44—4.40(m, 1H), 4.12—4.10(m, 1H), 3.63—3.60(m, 1H), 2.83—2.77(m, 1H), 2.71—2.68(m, 1H) | 161.3, 157.2, 138.8, 137.8, 136.6, 136.2, 135.0, 134.5(d, J=8.6 Hz), 133.9(d, J=9.2 Hz), 128.9, 128.8, 127.4, 127.3, 127.2(d, J=2.5 Hz), 127.1(d, J=1.9 Hz), 126.8, 122.1, 118.3(d, J=4.4 Hz), 60.6(d, J=4.6 Hz), 54.3, 43.2(d, J=28.3 Hz), 39.5(d, J=15.8 Hz) | 47.2(d, J=32.2 Hz,1P), 38.1(d, J=32.2 Hz, 1P) |
Cat.11 | 8.21—8.16(m, 2H), 7.55—6.68(m, 31H), 5.86—5.79(m, 1H), 5.41—5.34(m, 1H), 5.74—5.71(m, 1H), 4.56—4.52(m, 1H), 3.91—3.87(m, 1H), 3.78—3.70(m, 1H), 2.57—2.52(m, 1H), 2.45(m, 3H) | 165.2, 162.8, 139.1(d, J=16.4 Hz), 138.2, 137.8, 136.7, 135.7(d, J=8.9 Hz), 134.5(d, J=7.9 Hz), 129.3, 129.1, 128.7, 127.2(d, J=8.9 Hz), 127.0, 123.5, 119.4, 63.9(d, J=6.2 Hz), 56.5, 46.4(d, J=28.7 Hz), 29.4 | 43.4(d, J=33.9 Hz,1P), 37.3(d, J=34.8Hz, 1P) |
Cat.12 | 8.47—8.45(m, 1H), 7.88—7.84(m, 2H), 7.75—7.73(m, 2H), 7.66—7.62(m, 1H), 7.58—7.56(m, 2H), 7.52—7.07(m, 28H), 5.83—5.77(m, 1H), 5.63—5.56(m, 1H), 5.00—4.92(m, 1H), 4.63—4.57(m, 1H), 3.48—3.40(m, 1H), 2.96—2.89(m, 1H) | 163.4, 148.2, 139.0, 138.8, 138.0, 137.7, 136.9, 135.1(d, J=9.9 Hz), 134.0(d, J=9.1 Hz), 130.8, 129.3, 129.0(d, J=5.8 Hz), 128.7, 127.9, 127.4, 127.3, 127.2, 127.1, 126.2(d, J=2.0 Hz), 125.0, 119.8, 64.3(d, J=5.9 Hz), 52.4, 46.8(d, J=26.0 Hz) | 47.7(d, J=30.0 Hz,1P), 37.2(d, J=30.9 Hz, 1P) |
Entry | Cat. | Conversion(%) | e. e.(%) |
---|---|---|---|
1 | Cat.1 | >99 | 51 |
2 | Cat.2 | >99 | 54 |
3 | Cat.3 | >99 | 58 |
4 | Cat.4 | >99 | 65 |
5 | Cat.5 | 45 | 66 |
6 | Cat.6 | >99 | 24 |
7b | Cat.7 | >99 | 60 |
8b | Cat.8 | >99 | 60 |
9 | Cat.9 | >99 | 71 |
10 | Cat.10 | 23 | 69 |
11 | Cat.11 | 9 | ― |
12 | Cat.12 | 47 | 53 |
Table 4 Optimizationof catalystsa
Entry | Cat. | Conversion(%) | e. e.(%) |
---|---|---|---|
1 | Cat.1 | >99 | 51 |
2 | Cat.2 | >99 | 54 |
3 | Cat.3 | >99 | 58 |
4 | Cat.4 | >99 | 65 |
5 | Cat.5 | 45 | 66 |
6 | Cat.6 | >99 | 24 |
7b | Cat.7 | >99 | 60 |
8b | Cat.8 | >99 | 60 |
9 | Cat.9 | >99 | 71 |
10 | Cat.10 | 23 | 69 |
11 | Cat.11 | 9 | ― |
12 | Cat.12 | 47 | 53 |
1 | Gu X., Li X., Xie J., Zhou Q., Acta Chim. Sinica, 2019, 77(7), 598—612 |
2 | Zhou Y., Khan R., Fan B., Xu L., Synthesis⁃Stuttgart, 2019, 51(12), 2491—2505 |
3 | Werkmeister S., Junge K., Beller M., Org. Process Res. Dev., 2014, 18(2), 289—302 |
4 | Clarke M. L., Catal. Sci.Technol., 2012, 2(12), 2418—2423 |
5 | Kuriyama W., Matsumoto T., Ogata O., Ino Y., Aoki K., Tanaka S., Ishida K., Kobayashi T., Sayo N., Saito T., Org. Process Res. Dev., 2012, 16(1), 166—171 |
6 | Gao S., Tang W., Zhang M., Wang C., Xiao J., Synlett, 2016, 27(11), 1748—1752 |
7 | Chen S., Shi Y. H., Wang M., Chem. Asian J., 2018, 13(17), 2184—2194 |
8 | Bhat V., Welin E. R., Guo X., Stoltz B. M., Chem. Rev., 2017, 117(5), 4528—4561 |
9 | Li P., Hu X., Dong X. Q., Zhang X., Molecules, 2016, 21(10), 1327—1340 |
10 | Noyori R., Ikeda T., Ohkuma T., Widhalm M., Kitamura M., Takaya H., Akutagawa S., Sayo N., Saito T., Taketomi T., Kumobayashi H., J. Am. Chem. Soc., 1989, 111(25), 9134—9135 |
11 | Echeverria P. G., Ayad T., Phansavath P., Ratovelomanana⁃Vidal V., Synthesis⁃Stuttgart, 2016, 48(16), 2523—2539 |
12 | Xie J. H., Zhou Q. L., Aldrichimica Acta, 2015, 48(2), 33—40 |
13 | Swamy C. A. P., Varenikov A., de Ruiter G., Chem. Eur. J., 2020, 26(11), 2333—2337 |
14 | Zhou Z. T., Xie J. H., Zhou Q. L., Adv. Synth. Catal., 2009, 351(3), 363—366 |
15 | Xie J. H., Zhou Z. T., Kong W. L., Zhou Q. L., J. Am. Chem. Soc., 2007, 129(7), 1868—1869 |
16 | Zatolochnaya O. V., Rodriguez S., Zhang Y., Lao K. S., Tcyrulnikov S., Li G., Wang X. J., Qu B., Biswas S., Mangunuru H. P. R., Rivalti D., Sieber J. D., Desrosiers J. N., Leung J. C., Grinberg N., Lee H., Haddad N., Yee N. K., Song J. J., Kozlowski M. C., Senanayake C. H., Chem. Sci., 2018, 9(19), 4505—4510 |
17 | Liu C., Xie J. H., Li Y. L., Chen J. Q., Zhou Q. L., Angew. Chem. Int. Ed., 2013, 52(2), 593—596 |
18 | Li X., Zhao Z. B., Chen M. W., Wu B., Wang H., Yu C. B., Zhou Y. G., Chem. Commun., 2020, 56(43), 5815—5818 |
19 | Lu B., Wu X., Li C., Ding G., Li W., Xie X., Zhang Z., J. Org. Chem., 2019, 84(6), 3201—3213 |
20 | Gu G., Lu J., Yu O., Wen J., Yin Q., Zhang X., Org. Lett., 2018, 20(7), 1888—1892 |
21 | Hou C. J., Hu X. P., Org. Lett., 2016, 18(21), 5592—5595 |
22 | Echeverria P. G., Ferard C., Cornil J., Guerinot A., Cossy J., Phansavath P., Ratovelomanana⁃Vidal V., Synlett, 2014, 25(19), 2761—2764 |
23 | Hamada Y., Makino K., J. Synth. Org. Chem. Jpn., 2008, 66(11), 1057—1065 |
24 | Tao X., Li W., Li X., Xie X., Zhang Z., Org. Lett., 2013, 15(1), 72—75 |
25 | Prevost S., Gauthier S., de Andrade M. C. C., Mordant C., Touati A. R., Lesot P., Savignac P., Ayad T., Phansavath P., Ratovelomanana⁃Vidal V., Genet J. P., Tetrahedron⁃Asymmetry, 2010, 21(11—12), 1436—1446 |
26 | Fan D., Lu J., Liu Y., Zhang Z., Liu Y., Zhang W., Tetrahedron, 2016, 72(35), 5541—5547 |
27 | Seo Y. J., Kim J. A., Lee H.K ., J. Org. Chem., 2015, 80(17), 8887—8902 |
28 | Jones S., Zhao P., Tetrahedron⁃Asymmetry, 2014, 25(3), 238—244 |
29 | Kim J. A., Seo Y. J., Kang S., Han J., Lee H. K., Chem. Commun., 2014, 50(89), 13706—13709 |
30 | Chen M. W., Cai X. F., Chen Z. P., Shi L., Zhou Y. G., Chem. Commun., 2014, 50(83), 12526—12529 |
31 | Shi L., Ye Z. S., Cao L. L., Guo R. N., Hu Y., Zhou Y. G., Angew. Chem. Int. Ed., 2012, 51(33), 8286—8289 |
32 | Liu B., Song R., Xu J., Majhi P. K., Yang X., Yang S., Jin Z., Chi Y. R., Org. Lett., 2020, 22(9), 3335—3338 |
33 | Chen X., Fong J. Z. M., Xu J., Mou C., Lu Y., Yang S., Song B. A., Chi Y. R., J. Am. Chem. Soc., 2016, 138(23), 7212—7215 |
34 | Yamamoto E., Wakafuji K., Furutachi Y., Kobayashi K., Kamachi T., Tokunaga M., ACS Catal., 2018, 8(7), 5708—5713 |
35 | Hu L., Zhang Y., Chen G. Q., Lin B. J., Zhang Q. W., Yin Q., Zhan X., Org. Lett., 2019, 21(14), 5575—5580 |
36 | Endean R. T., Rasu L., Bergens S. H., ACS Catal., 2019, 9(7), 6111—6117 |
37 | Cao B., Wang Y., Ding K., Neamati N., Long Y. Q., Org. Biomol. Chem., 2012, 10(6), 1239—1245 |
38 | Faulkner A. D., Kaner R. A., Abdallah Q. M. A., Clarkson G., Fox D. J., Gurnani P., Howson S. E., Phillips R. M., Roper D. I., Simpson D. H., Scott P., Nat. Chem., 2014, 6(9), 797—803 |
39 | Ding X., Tian C., Hu Y., Gong L., Meggers E., Eur. J. Org. Chem., 2016, 2016(5), 887—890 |
40 | Kawamura K., Fukuzawa H., Hayashi M., Bull. Chem. Soc. Jpn., 2011, 84(6), 640—647 |
41 | Spasyuk D., Gusev D. G., Organometallics, 2012, 31(15), 5239—5242 |
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