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Asymmetric Synthesis, BINAPs, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Privileged Ligands and Complexes 


(R)-DM-BINAP has application in :

1. Copper-catalyzed asymmetric Mannich-type reactions of N-acylimino esters (Ref: J. Am. Chem. Soc., 2003, 125, 2507)

2. Enantioselective fluorination of oxindoles (Ref: J. Am. Chem. Soc., 2005, 127, 10164)

3. [2+2+2] cycloaddition of tetraynes and hexaynes (Ref: Tetrahedron, 2008, 64, 821)

4. Asymmetric reduction of ketones via ruthenium-catalyzed transfer hydrogenation (Ref: J. Am. Chem. Soc., 2011, 133, 10696)

5. Asymmetric hydroboration of unsaturated imines (Ref: Org. Lett., 2013, 15, 4810)

Note: Please see applications of (R)-BINAP and (R)-T-BINAP for additional applications in which these ligands may be used

CAS Number
(R)-(+)-1,1′-Binaphthalene-2,2′-diyl)bis[bis(3,5-dimethylphenyl)phosphine], (R)-(+)-2,2′-Bis[di(3,5-xylyl)phosphino]-1,1′-binaphthyl
Molecular Formula
MDL Number
Chemical Name
Molecular Weight
Melting Point
187 - 191 °C
1 gm, 10 Gm & 50 gm in Glass Bottles, Bigger packaging available on request.
White to light yellow

Price and Availability

QuantityAvailability*Price (INR)
1 gmIn StockOn Request
10 gmIn StockOn Request
50 gmIn StockOn Request
1 kg4-5 WeeksOn Request
25 kg8-10 Weeks (Negotiable)On Request

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(R)-DM-BINAP  | Synthesis with Catalysts


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