Highly chemoselective 2,4,5-triaryl-1,3-dioxolane formation from intermolecular 1,3-dipolar addition of carbonyl ylide with aryl aldehydes

Organic Letters

Volumn 6, Issue 18, 2004, Pages 3071-3074

  Lu, Chong Dao ^a   Chen, Zhi Yong ^a   Liu, Hui ^a   Hu, Wen Hao ^a   Mi, Ai Qiao ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; ACETIC ACID DERIVATIVE; ALDEHYDE DERIVATIVE; RHODIUM;

ADDITION REACTION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; ELECTRON; REACTION ANALYSIS; STRUCTURE ANALYSIS;

EID: 4544324323     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0489494     Document Type: Article

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35. Even though 2,4-dinitrobenzaldehyde served as a good dipolarophile, reaction of diazo 1 with 2,4-dinitrobenzaldehyde alone still gave only epoxide product without trace amounts of dioxolane; see the Supporting Information.