ChemInform Abstract: A Highly Enantioselective One-Pot Sulfur Ylide Epoxidation Reaction.

ChemInform ◽  
2010 ◽  
Vol 33 (42) ◽  
pp. no-no
Author(s):  
Caroline L. Winn ◽  
Benjamin R. Bellenie ◽  
Jonathan M. Goodman
Keyword(s):  
One Pot ◽  
Epoxidation Reaction ◽  
Sulfur Ylide

A highly enantioselective one-pot sulfur ylide epoxidation reaction

2002 ◽  
Vol 43 (31) ◽  
pp. 5427-5430 ◽  
Author(s):  
Caroline L. Winn ◽  
Benjamin R. Bellenie ◽  
Jonathan M. Goodman
Keyword(s):  
One Pot ◽  
Epoxidation Reaction ◽  
Sulfur Ylide

ChemInform Abstract: Solvent Effect on Sulfur Ylide Mediated Epoxidation Reaction.

ChemInform ◽  
2008 ◽  
Vol 39 (13) ◽  
Author(s):  
Hee-Yoon Lee ◽  
Imhyuck Bae ◽  
Kyung-Hyun Min
Keyword(s):  
Solvent Effect ◽  
Epoxidation Reaction ◽  
Sulfur Ylide

Sulfur Ylide Initiated [4 + 1]/[4 + 2] Annulation Reactions: A One-Pot Approach to Dibenzofuran Acrylate Derivatives

2019 ◽  
Vol 21 (16) ◽  
pp. 6370-6373 ◽  
Author(s):  
Jiaan Shao ◽  
Wenteng Chen ◽  
Zhimin Ying ◽  
Shuangrong Liu ◽  
Feng Luo ◽  
...  
Keyword(s):  
One Pot ◽  
Sulfur Ylide

A rapid, microwave-assisted, one-pot cyclopropanation reaction to synthesize (4-ferrocenyl)benzoylcyclopropane in the solid state

2005 ◽  
Vol 83 (12) ◽  
pp. 2140-2143 ◽  
Author(s):  
Juxing Yin ◽  
Xiaolong Li ◽  
Xiaoli Wu ◽  
Baohua Chen ◽  
Zenglu Liu ◽  
...  
Keyword(s):  
Reaction Time ◽  
Solid State ◽  
Environmental Pollution ◽  
Intermediate Product ◽  
One Pot ◽  
Microwave Assisted ◽  
Sulfur Ylide

Some new (4-ferrocenyl)benzoylcyclopropanes were prepared rapidly via a microwave-assisted, one-pot cyclopropanation reaction in the solid state, directly using 4-ferrocenylacetophenone, aldehyde, and sulfur ylide as the starting materials. The main advantages of this procedure are convenient operation, shorter reaction time, lower environmental pollution, and no need to isolate the intermediate product (chalcone) in a separate step.Key words: 4-ferrocenylacetophenone, sulfur ylide, microwave-assisted, one-pot, solid state.

Formal [4+2] annulation of enaminones and cyanomethyl sulfur ylide: one-pot access to polysubstituted pyridin-2(1H)-ones

2014 ◽  
Vol 50 (97) ◽  
pp. 15378-15380 ◽  
Author(s):  
Qian Zhang ◽  
Xu Liu ◽  
Xiaoqing Xin ◽  
Rui Zhang ◽  
Yongjiu Liang ◽  
...  
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Nucleophilic Vinylic Substitution ◽  
Vinylic Substitution ◽  
Sulfur Ylide ◽  
Nucleophilic Cyclization

One-pot synthesis of polysubstituted pyridin-2(1H)-ones by formal [4+2] annulation of enaminones and cyanomethyl sulfur ylide is described involving sequential nucleophilic vinylic substitution, intramolecular nucleophilic cyclization and dealkylation reactions.

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