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| Product | Description | |
|---|---|---|
| (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine | (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine. Uses: Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines. nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes. enantioselective reduction of prochiral ketones with nabh4/me2so4/(s)-me-cbs. Group: other electronic materials. Alternative Names: AKOS015840981; (S)-1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole; MFCD00078439; (S)- Methyl-CBS-oxazaborolidine; ZINC169743318; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3 H-pyrrolo[1,2-c][1,3,2] oxazaborole; (S)-1-methyl-3,3-diphenylhexahydropyrrolo-[1,2-c][1,3,2]oxazaborole; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3H-pyrrolo[1,2-c]-[1,3,2]oxazaborole; (S)-Me-CBS; Corey catalyst. CAS No. 112022-81-8. Product ID: (3aS)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole. Molecular formula: 277.174g/mol. Mole weight: C18H20BNO. B1 (N2CCCC2C (O1) (C3=CC=CC=C3)C4=CC=CC=C4)C. InChI=1S / C18H20BNO / c1-19-20-14-8-13-17 (20) 18 (21-19, 15-9-4-2-5-10-15) 16-11-6-3-7-12-16 / h2-7, 9-12, 17H, 8, 13-14H2, 1H3 / t17- / m0 / s1. VMKAFJQFKBASMU-KRWDZBQOSA-N. |  |
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