Regioselective Ring-opening Reaction of 1,2-Epoxides with Arylselenol under Solvent-free Conditions and Application to the Synthesis of 1,3-Oxazolidin-2-ones-Reference-Cited by-同舟云学术

Regioselective Ring-opening Reaction of 1,2-Epoxides with Arylselenol under Solvent-free Conditions and Application to the Synthesis of 1,3-Oxazolidin-2-ones

Published:2006-05 Issue:5 Volume:24 Page:669-673
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Yang Ming-Hua,Yuan Chao-Ying,Pan Yi,Zhu Cheng-Jian

Publisher

Wiley

Subject

General Chemistry

Reference31 articles.

1. Generation and Mesolytic Dynamics of Organoselenane and Selenosilane Radical Ions: Development of Mechanistically Interesting and Synthetically Useful Chemistry

2. Selenocyclizations: Control by Coordination and by the Counterion

3. Tetrathiomolybdate Assisted Epoxide Ring Opening with Masked Thiolates and Selenoates: Multistep Reactions in One Pot

4. Highly Enantioselective Reaction of α-Selenoorganolithium Compounds with Chiral Bis(oxazoline)s and Preparation of Enantioenriched Benzylidencyclohexanes

5. Chemistry of Biologically Important Synthetic Organoselenium Compounds

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