(+)-B-Methoxydiisopinocampheylborane,

Code: 317039-5G D2-231

Application

Both (+)- and (-)-forms are precursors to B-allyldiisopinocampheylborane derivatives, which are subsequently reacted with aldehydes to give homoallylic a...


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€103.60 5G
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Application

Both (+)- and (-)-forms are precursors to B-allyldiisopinocampheylborane derivatives, which are subsequently reacted with aldehydes to give homoallylic alcohols and β-amino alcohols of high enantiomeric excess.

Reactant involved in: Oxidative cyclization and alkylation for synthesis of ionomycin Intramolecular conjugate addition for tetrahydropyran synthesis Aldol addition and Suzuki coupling reactions Allylation Synthesis of alkanols

Packaging

5, 25, 100 g in glass bottle

formsolid
InChI keyIAQXEQYLQNNXJC-JPDDNCELSA-N
InChI1S/C21H37BO/c1-12-16-8-14(20(16,3)4)10-18(12)22(23-7)19-11-15-9-17(13(19)2)21(15,5)6/h12-19H,8-11H2,1-7H3/t12-,13-,14+,15+,16-,17-,18-,19-/m0/s1
Quality Level100
SMILES stringCOB([C@H]1CC2CC([C@@H]1C)C2(C)C)[C@H]3CC4CC([C@@H]3C)C4(C)C
Cas Number99438-28-5
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