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. Author manuscript; available in PMC: 2017 Jun 6.
Published in final edited form as: Chemistry. 2016 May 3;22(24):8158–8166. doi: 10.1002/chem.201600674

Scheme 1.

Scheme 1

Synthesis of allylsilane 9. a) TESOTf, 2,6-lutidine, DCM, 0 °C, 85%; b) LiCH2TMS, pentane, 0 °C, 98%; c) KHMDS, PhNTf2, THF, −78 °C, 91%; d) ClMgCH2TMS, Pd(PPh3)4, Et2O, 0 °C, 81%; e) CSA, MeOH, RT, 75%; DCM=dichloromethane; THF=tetrahydrofuran; TESOTf=triethylsilyl trifluoromethanesulfonate; KHMDS=potassium bis(trimethylsilyl)amide; PhNTf2=N-phenyl-bis(trifluoromethanesulfonimide); CSA=10-camphorsulfonic acid.