Stereoselection in iodolactonisations of 3-silyloxy-5-alkenoic acids
摘要:
Iodolactonisations of (Z)- or (E) 3 silyloxy-5-alkenoic acids [1 and 7] both lead to trans-disubstituted valerolactones [6 and 8]. which differ only in the stereochemistry of the iodine substituent.
Stereoselection in iodolactonisations of 3-silyloxy-5-alkenoic acids
摘要:
Iodolactonisations of (Z)- or (E) 3 silyloxy-5-alkenoic acids [1 and 7] both lead to trans-disubstituted valerolactones [6 and 8]. which differ only in the stereochemistry of the iodine substituent.
Stereoselection in iodolactonisations of 3-silyloxy-5-alkenoic acids
作者:Simon B. Bedford、Garry Fenton、David W. Knight、Duncan Shaw
DOI:10.1016/s0040-4039(00)79027-7
日期:1992.10
Iodolactonisations of (Z)- or (E) 3 silyloxy-5-alkenoic acids [1 and 7] both lead to trans-disubstituted valerolactones [6 and 8]. which differ only in the stereochemistry of the iodine substituent.