Bisphosphine ligand

Organic compounds -- part of the class 532-570 series – Organic compounds – Phosphorus containing

Reexamination Certificate

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C502S326000

Reexamination Certificate

active

07569730

ABSTRACT:
A compound represented by the following general formula (I):[wherein R1represents hydrogen atom, or an alkyl group, R2represents a hydroxyalkyl group, or a triarylmethyloxyalkyl group, or R1and R2combine together to represent —C(R3)(R4)— (R3and R4represent hydrogen atom, an alkyl group, or hydroxyl group, or R3and R4may combine together to represent oxo group), or —C(R5)(R6)—O—C(R7)(R8)— (R5to R8represent hydrogen atom, an alkyl group, or hydroxyl group, or R5and R6may combine together to represent oxo group, and R7and R8may combine together to represent oxo group); Ar1to Ar4independently represent an aryl group (the aryl group may have 1 to 5 of the same or different substituents), *1 to *4 indicate asymmetric carbons, and configurations are cis between *1 and *2, cis between *3 and *4, and trans between *2 and *3]. An optically active phosphine ligand which can be easily synthesized and gives a transition metal complex showing superior asymmetric catalyst activity is provided.

REFERENCES:
patent: 2005/0288523 (2005-12-01), Knochel et al.
patent: 1 595 885 (2005-11-01), None
patent: 2005-336181 (2005-12-01), None
patent: 91/17998 (1991-11-01), None
patent: 93/01199 (1993-01-01), None
English Language Abstract of JP 2005-336181 (provided by Esp@cenet).
Catalytic Asymmetric Synthesis, Second Edition, Ed., Iwao Ojima, Wiley-VCH, pp. v-vii, ix-xiv, 1, and 797-99 (2000).
Inoguchi et al., “Development of a New Six-Membered Chelating Chiral [Bisphosphine]rhodium Catalyst and Efficient Asymmetric Hydrogenation of (Z)-2-Acetamidocinnamic Acid”SYNLETT49-51 (1991).
Corey et al., “Stereo-Controlled Synthesis of Prostaglandins F2αand E2(dl)”J. Am. Chem. Soc., vol. 91, No. 20, pp. 5675-5677 (1969).
“Organic Metal Complex” Jikken Kagaku Koza (Lecture of Experimental Chemistry), 4th edition, edited by the Chemical Society of Japan, vol. 18, pp. 338-345 (1991) Maruzen, along with a partial English language translation.
M. Kitamura,Org. Synth., vol. 71, pp. 1-13 (1993).
F. Sato, Gosei Kagakusha no tameno Jikken Yuki Kinzoku Kagaku (Experimental Organic Metal Chemistry for Synthetic Chemists), pp. 195-196, Kodansha (1992), along with a partial English language translation.
“Organic Metal Complex” Jikken Kagaku Koza (Lecture of Experimental Chemistry), 4th edition, edited by the Chemical Society of Japan, vol. 18, p. 362-364 (1991), along with a partial English language translation.

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