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(S)-2-Methyl-CBS-oxazaborolidine is used as an oxazaborolidine catalyst. It is also employed in the asymmetric reduction of prochiral ketones. Other applications include the enantioselective synthesis of α-hydroxy acids, α-amino acids, C2-symmetrical ferrocenyl diols and propargyl alcohols. It is an anhydrous catalyst for 'CBS' reduction reaction.
Panayiotis A Procopiou.; Gillian E Morton.; Martin Todd.; Graham Webb. Enantioselective synthesis of (S)-salmeterol via asymmetric reduction of azidoketone by Pichia angusta. Tetrahedron: Asymmetry. 2001, 12 (14), 2005-2008.
Toshiyasu Takemoto.; Katsuyoshi Nakajima.; Yukiko Iio, Masakazu Tamura.; Takahide Nishi. Asymmetric synthesis of enantiomerically pure spiro[((2S)-hydroxy)indane-1,4?-piperidine]. Tetrahedron: Asymmetry. 1999, 10 (9), 1787-1793.
Anhydrous catalyst for 'CBS' reduction reaction. For examples of use in asymmetric reduction of ketones, see: Org. Synth. Coll., 9, 362, 676 (1998). For further information, see (S)-2-Methyl-CBS-oxazaborolidine monohydrate, L09219.
Hazard Statements: H225-H302-H333-H315-H361-H336-H373-H304
Highly flammable liquid and vapour. Harmful if swallowed. May be harmful if inhaled. Causes skin irritation. Suspected of damaging fertility or the unborn child. May cause drowsiness or dizziness. May cause damage to organs through prolonged or repeated exposure. May be fatal if swallowed and enters airways.
Precautionary Statements: P210-P260-P301+P310a-P303+P361+P353-P405-P501a
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Do not breathe dust/fume/gas/mist/vapours/spray. IF SWALLOWED: Immediately call a POISON CENTER/doctor IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.