| Identification | Back Directory | [Name]
(-)-B-METHOXYDIISOPINOCAMPHEYLBORANE | [CAS]
99438-28-5 | [Synonyms]
(+)-B-methoxydiisocamphenylborane
(+)-B-methoxydiisocamphenylborane
(-)-B-METHOXYDIISOPINOCAMPHEYLBORANE
(+)-B-Methoxydiisopinocampheylborane
(-)-DIISOPINOCAMPHEYLMETHOXYBORANE HYDRATE
(+)-B-methoxydiisopinocampheylborane hydrate
(-)-B-METHOXYDIISOPINOCAMPHEYLBORANE HYDRATE
(-)-beta-Methoxydiisopinocampheylboranehydrate
cis-1,2,3,4-Tetrahydro-2-phenyl-1-naphthaleneaceticaci
(+)-B-Methoxydiisopinocampheylborane,(+)-Diisopinocampheylmethoxyborane
Methoxybis((1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-yl)borane
Borinic acid, B,B-bis[(1S,2R,3S,5S)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-, methyl ester | [Molecular Formula]
C21H37BO | [MDL Number]
MFCD21332906 | [MOL File]
99438-28-5.mol | [Molecular Weight]
316.33 |
| Hazard Information | Back Directory | [Uses]
(-)-B-Methoxydiisopinocampheylborane hydrate is an intermediate used in the synthesis of homoallylic alcohol''s and several complex natural products. | [Uses]
(+)?-?B-?Methoxydiisopinocamp?heylborane is a chiral catalyst used in synthetic organic chemistry such as the bacterial macrolide glycoside (-?)?-?Lyngbyaloside B which maintains antiproliferative activity. | [Uses]
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
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