Facile Conversion of Epoxides to 1,2-Diacetates with NaOAc•3H2O/Ac2O System

Authors

  • Behzad Zeynizadeh Department of Chemistry, Faculty of Science, Urmia University, P.O. Box 5756151818 Urmia, I.R. IRAN
  • Masumeh Gilanizadeh Department of Chemistry, Faculty of Science, Urmia University, P.O. Box 5756151818 Urmia, I.R. IRAN
Abstract:

  This study represents a highly efficient and regioselective ring-opening of epoxides with acetic anhydride in the presence of NaOAc·3H2O at solvent-free conditions. The ring-opening of different classes of epoxides were carried in oil bath (70-80 °C) to afford 1,2-diacetates in high to excellent yields

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

facile conversion of epoxides to 1,2-diacetates with naoac•3h2o/ac2o system

this study represents a highly efficient and regioselective ring-opening of epoxides with acetic anhydride in the presence of naoac·3h2o at solvent-free conditions. the ring-opening of different classes of epoxides were carried in oil bath (70-80 °c) to afford 1,2-diacetates in high to excellent yields

full text

Disulfide catalyzed the highly regioselective conversion of epoxides to halohydrins with elemental halogens

The regioselective ring opening of styrene oxide using elemental iodine and bromine in the presence of disulfides as new catalysts was studied. The conductivity titration and UV spectroscopy were used to study the interaction of iodine with these catalysts. The results indicate that disulfide 11 is efficient in polyiodide formation, and can catalyze this reaction in excellent yield and high reg...

full text

Disulfide catalyzed the highly regioselective conversion of epoxides to halohydrins with elemental halogens

The regioselective ring opening of styrene oxide using elemental iodine and bromine in the presence of disulfides as new catalysts was studied. The conductivity titration and UV spectroscopy were used to study the interaction of iodine with these catalysts. The results indicate that disulfide 11 is efficient in polyiodide formation, and can catalyze this reaction in excellent yield and high reg...

full text

disulfide catalyzed the highly regioselective conversion of epoxides to halohydrins with elemental halogens

the regioselective ring opening of styrene oxide using elemental iodine and bromine in the presence of disulfides as new catalysts was studied. the conductivity titration and uv spectroscopy were used to study the interaction of iodine with these catalysts. the results indicate that disulfide 11 is efficient in polyiodide formation, and can catalyze this reaction in excellent yield and high reg...

full text

stability and attraction domains of traffic equilibria in day-to-day dynamical system formulation

در این پژوهش مسئله واگذاری ترافیک را از دید سیستم های دینامیکی فرمول بندی می کنیم.فرض کرده ایم که همه فاکتورهای وابسته در طول زمان ثابت باشند و تعادل کاربر را از طریق فرایند منظم روزبه روز پیگیری کنیم.دینامیک ترافیک توسط یک نگاشت بازگشتی نشان داده می شود که تکامل سیستم در طول زمان را نشان می دهد.پایداری تعادل و دامنه جذب را توسط مطالعه ویژگی های توپولوژیکی تکامل سیستم تجزیه و تحلیل می کنیم.پاید...

Facile Palladium-Mediated Conversion of Ethanethiol Esters to

O tratamento de ésteres etanotiólicos com trietilsilano e paládio sobre carbono, a temperatura ambiente, fornece aldeídos. Adicionalmente, uma variedade de cetonas foram preparadas por reações de ésteres etanotiólicos com reagentes organozinco catalisados por paládio. Vários grupos funcionais, incluindo ésteres, cetonas, haletos aromáticos e aldeídos são tolarados em ambas as tarnsformações. Es...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 35  issue 1

pages  25- 29

publication date 2016-02-01

By following a journal you will be notified via email when a new issue of this journal is published.

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023