BINAP
BINAP | |
---|---|
![]() | |
IUPAC (2R,3S)-2,2'- | |
BINAP | |
CAS |
76189-55-4(R) ![]() 76189-56-5(S) ![]() |
C44H32P2 | |
622.67 g·mol⁻¹ | |
熔點 | 239-241 °C (R), 238-240 °C (S) |
![](https://upload.wikimedia.org/wikipedia/commons/thumb/a/a0/BINAP_3D.png/220px-BINAP_3D.png)
BINAP
應用
[這種
製 備
[BINAP
BINOL
參考 文獻
[- ^ Kitamura, Masato; M. Tokunaga, T. Ohkuma, and R. Noyori. Asymmetric hydrogenation of 3-oxo carboxylates using BINAP-ruthenium complexes. Org. Syn. 1998, 9: 589 [2011-05-06]. (
原始 內容存 檔於2011-07-18). - ^ Akutagawa, S. A practical synthesis of (-)-menthol with the Rh-BINAP catalyst. Chirality Ind. 1992: 313−323.
- ^ Kumobayashi, Hidenori; Sayo, Noboru; Akutagawa, Susumu; Sakaguchi, Toshiaki; and Tsuruta, Haruki. Industrial asymmetric synthesis by use of metal-BINAP catalysts. Nippon Kagaku Kaishi. 1997, 12: 835−846.
- ^ BINAP: An industrial approach to manufacture (PDF). Rhodia (company). [2008-10-20]. (
原始 內容存 檔 (PDF)於2007-09-29). - ^ Cai, Dongwei; J. F. Payack, D. R. Bender, D. L. Hughes, T. R. Verhoeven, and P. J. Reider. (R)-(+)- and (S)-(−)-2,2'-bis(diphenylphosphino)-1,1'-binapthyl (BINAP). Org. Syn. 2004, 10: 112 [2011-05-06]. (
原始 內容存 檔於2011-07-18). - ^ Nakajima, Makoto; S. Kotani, T. Ishizuka, S. Hashimoto. Chiral Phosphine Oxide BINAPO as a Catalyst for Enantioselective Allylation of Aldehydes with Allyltrichlorosilanes. ChemInform. 2005, 36. doi:10.1002/chin.200516031.