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(R)-3,3'-Bis(4-(1,1-dimethylethyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate | 861909-30-0

(R)-3,3'-Bis(4-(1,1-dimethylethyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate
(R)-3,3'-Bis(4-(1,1-dimethylethyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate
861909-30-0
C40H37O4P
612.693152189255
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:(R)-3,3'-Bis(4-(1,1-dimethylethyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate结构式
名称和标识符
MDL MFCD27920532
InChIKey NLMLOSHPJMFGTF-UHFFFAOYSA-N
Inchi 1S/C40H37O4P/c1-39(2,3)29-19-15-25(16-20-29)33-23-27-11-7-9-13-31(27)35-36-32-14-10-8-12-28(32)24-34(38(36)44-45(41,42)43-37(33)35)26-17-21-30(22-18-26)40(4,5)6/h7-24H,1-6H3,(H,41,42)
SMILES O=P1(OC2C(C3C=CC(C(C)(C)C)=CC=3)=CC3C(C=2C2C(=C(C4C=CC(C(C)(C)C)=CC=4)C=C4C=2C=CC=C4)O1)=CC=CC=3)O
别名信息
- 中文别名 -
  • (R)-3,3'-双(4-叔丁基苯基)-1,1'-联萘酚磷酸酯
  • (R)-3,3'-双(4-叔丁基苯基)-1,1'-联萘酚膦酸酯
- 英文别名 -
  • (R)-3,3'-Bis(4-(1,1-dimethylethyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate
  • (11bR)-2,6-Bis[4-(1,1-dimethylethyl)phenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
合成路线

合成路线:6 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:4 步

反应条件:
参考文献:
Enantioselective Organocatalytic Fluorination-Induced Wagner-Meerwein Rearrangement
Romanov-Michailidis, Fedor; et al, Angewandte Chemie, 2013, 52(35), 9266-9270

合成路线:6 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:6 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:6 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:5 步

反应条件:
参考文献:
Enantioselective Organocatalytic Fluorination-Induced Wagner-Meerwein Rearrangement
Romanov-Michailidis, Fedor; et al, Angewandte Chemie, 2013, 52(35), 9266-9270

合成路线:2 步

反应条件:
参考文献:
A Protecting-Group-Free Route to Chiral BINOL-Phosphoric Acids
Li, Bao-Jian; et al, European Journal of Organic Chemistry, 2011, 2011(20-21), 3932-3937

合成路线:6 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:5 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:1 步

反应条件:
参考文献:
Bronsted Acid-Catalyzed Regioselective Carboxamidation of 2-Indolylmethanols with Isonitriles
Chaudhari, Tohasib Yusub; et al, Journal of Organic Chemistry, 2023, 88(15), 10412-10425

合成路线:1 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:2 步

反应条件:
参考文献:
Catalytic Enantioselective Nazarov Cyclization: Construction of Vicinal All-Carbon-Atom Quaternary Stereocenters
Jolit, Anais; et al, Angewandte Chemie, 2014, 53(24), 6180-6183

合成路线:3 步

反应条件:
参考文献:
Catalytic Enantioselective Nazarov Cyclization: Construction of Vicinal All-Carbon-Atom Quaternary Stereocenters
Jolit, Anais; et al, Angewandte Chemie, 2014, 53(24), 6180-6183

合成路线:2 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:3 步

反应条件:
参考文献:
Enantioselective Organocatalytic Fluorination-Induced Wagner-Meerwein Rearrangement
Romanov-Michailidis, Fedor; et al, Angewandte Chemie, 2013, 52(35), 9266-9270

合成路线:4 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560

合成路线:1 步

反应条件:
参考文献:
A Protecting-Group-Free Route to Chiral BINOL-Phosphoric Acids
Li, Bao-Jian; et al, European Journal of Organic Chemistry, 2011, 2011(20-21), 3932-3937

合成路线:1 步

反应条件:
参考文献:
Enantioselective Organocatalytic Fluorination-Induced Wagner-Meerwein Rearrangement
Romanov-Michailidis, Fedor; et al, Angewandte Chemie, 2013, 52(35), 9266-9270

合成路线:3 步

反应条件:
参考文献:
Enantioselective Oxidative Homocoupling and Cross-Coupling of 2-Naphthols Catalyzed by Chiral Iron Phosphate Complexes
Narute, Sachin; et al, Journal of the American Chemical Society, 2016, 138(50), 16553-16560
(R)-3,3'-Bis(4-(1,1-dimethylethyl)phenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate推荐生产厂家
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