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Chemical Structure| 173603-23-1 Chemical Structure| 173603-23-1

Structure of 173603-23-1

Chemical Structure| 173603-23-1

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Product Details of [ 173603-23-1 ]

CAS No. :173603-23-1
Formula : C20H30B2O4
M.W : 356.07
SMILES Code : CC1(C)C(C)(C)OB(/C(C2=CC=CC=C2)=C\B3OC(C)(C)C(C)(C)O3)O1
MDL No. :MFCD02683500

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Application In Synthesis of [ 173603-23-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 173603-23-1 ]

[ 173603-23-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 173603-23-1 ]
  • [ 16355-00-3 ]
YieldReaction ConditionsOperation in experiment
86% Representative Procedure for ENANTIOSELECTIVE Hydrogenation of Alkenes A mono or diboronated ALKENE undergoes enantioselective hydrogenation in the presence of a chiral catalyst under 15 atm of pressure according to the first step of Scheme 4 to provide a diboronated adduct. The diboronated adduct is further reacted with hydrogen peroxide to provide (R)-1-PHENYL-1, 2-ETHANEDIOL at 86% yield and 93% enantiometic excess (ee). 2% Rh (nbd) BF4 B (pin 4% Walphos B (pin) H202 J, Ph
 

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