In situ generation and nucleophilic capture of 1,n-dial equivalents from 1,n-dioates (α,ω-diesters)

Synthesis

Volumn , Issue 10, 2006, Pages 1572-1574

  Hoye, Thomas R ^a   Kopel, Lucas C ^a   Ryba, Troy D ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Hydrides; Nucleophilic additions; Reductions; Tandem reactions; Wittig reactions

Indexed keywords

ALDEHYDES; ESTERS; HYDRIDES; OLEFINS; REDUCTION; SYNTHESIS (CHEMICAL);

NUCLEOPHILIC ADDITIONS; TANDEM REACTIONS; WITTIG REACTIONS;

AROMATIC COMPOUNDS;

1 N DIALDEHYDE; ALDEHYDE DERIVATIVE; ALLYLMAGNESIUM CHLORIDE; ALPHA,OMEGA DIESTER; CHLORIDE; DIISOBUTYLALUMINUM HYDRIDE; ESTER DERIVATIVE; GLUTARIC ACID; HYDROGEN; MALONALDEHYDE; PHOSPHONIC ACID DERIVATIVE; SUCCINIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; GRIGNARD REACTION; REDUCTION;

EID: 33744465052     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926465     Document Type: Article

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