Sigma-Aldrich
(S)-DTBM-SEGPHOS >=94% (C005B-025020)
Application Takasago Ligands and Complexes for Asymmetric Reactions Catalytic ligand for: Enantioselective synthesis of secondary allylic alcohols via enantioselective reductions of α,β-unsaturated ketones Stereoselective preparation of
Application
Takasago Ligands and Complexes for Asymmetric Reactions
Catalytic ligand for:
- Enantioselective synthesis of secondary allylic alcohols via enantioselective reductions of α,β-unsaturated ketones
- Stereoselective preparation of cyclohexanone derivatives via rhodium-catalyzed rearrangement of allyl or allenic cyclobutanols
- Cu-catalyzed asymmetric conjugate reduction of beta-substituted unsaturated phosphonates to give optically active beta-stereogenic alkylphosphonates
- Asymmetric synthesis of cyclohexenones via Rh-catalyzed desymmetrization through enantioselective C-C bond activation and ring expansion of allenyl cyclobutanols
- Enantioselective synthesis and crystal structure of P-stereogenic alkynylphosphine oxides by Rh-catalyzed [2+2+2] cycloaddition
Legal Information
Sold in collaboration with Takasago for research purposes only. JP Registration No. 3148136
SEGPHOS is a registered trademark of Takasago Intl. Corp.
Specifications
- UPC:
- 51273300
- Condition:
- New
- Weight:
- 1.00 Ounces
- HazmatClass:
- No
- Quantity:
- 1
- Unit of Measurement:
- GR
- MPN:
- 692980-1G
- CAS:
- 210169-40-7



