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It is used as pharmaceutical intermediate.
P.Veeraraghavan Ramachandran.; Baoqing Gong.; Aleksandar V. Teodorovic'.; Herbert C. Brown. Selective reductions. 52. Efficient asymmetric reduction of α-acetylenic α?-fluoroalkyl ketones with either B-chlorodiisopinocampheylborane or B-isopinocampheyl-9-borabicyclo[3.3.1]nonane in high enantiomeric purity. The influence of fluoro groups in such reductions.Tetrahedron: Asymmetry. 1994, 5 (6),1061-1074 .
M. Mark Midland.; Deborah C. McDowell.; Robert L. Hatch.; Alfonso Tramontano. Reduction of .alpha.,.beta.-acetylenic ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane. High asymmetric induction in aliphatic systems.J. Am. Chem. Soc. 1980, 102 (2),867-869 .
Hazard Statements: H315-H319
Causes skin irritation. Causes serious eye irritation.
Precautionary Statements: P280a-P264-P305+P351+P338-P321-P332+P313-P337+P313
Wear protective gloves and eye/face protection. Wash thoroughly after handling. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Specific treatment (see label). If skin irritation occurs: Get medical advice/attention. If eye irritation persists: