Thiomaleic anhydride: A convenient building block for the synthesis of α-substituted γ- and δ-lactones through free-radical addition, nucleophilic ring opening, and subsequent thiocarboxylate manipulation

Journal of Organic Chemistry

Volumn 74, Issue 17, 2009, Pages 6792-6796

  Crich, David ^a,b   Rahaman, Md Yeajur ^b  

^a INSTITUT DE CHIMIE DES SUBSTANCES NATURELLES   (France)

^b WAYNE STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACID RESIDUES; ALLYL PHENYL; BUILDING BLOCKES; CHEMICAL EQUATIONS; ELECTRON-DEFICIENT; FREE-RADICAL ADDITION; HIGH YIELD; NUCLEOPHILIC RING OPENING; PHENYLBORONIC ACIDS; RADICAL INITIATORS; THIOCARBOXYLATE; THIOESTERS; THIOPHENOLS; TRIMETHYLSILYL;

ALDEHYDES; CHEMICAL REACTIONS; INITIATORS (CHEMICAL); KETONES; ORGANIC ACIDS; SILANES; SULFUR COMPOUNDS;

AMIDES;

ACID ANHYDRIDE; ALDEHYDE; BENZENEBORONIC ACID; CARBOXYLIC ACID DERIVATIVE; FREE RADICAL; GAMMA LACTONE DERIVATIVE; KETONE; LACTONE DERIVATIVE; SULFONAMIDE; THIOESTER; THIOMALEIC ANHYDRIDE; THIOPHENOL; TRIMETHYLSILYL DERIVATIVE; TRIS(TRIMETHYLSILYL)SILANE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CYCLIZATION; REACTION ANALYSIS; RING OPENING; SYNTHESIS;

ALDEHYDES; AMIDES; ANHYDRIDES; BORONIC ACIDS; CARBOXYLIC ACIDS; CHEMISTRY, ORGANIC; ESTERS; FREE RADICALS; KETONES; LACTONES; SULFHYDRYL COMPOUNDS; SULFIDES;

EID: 69549110386     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901219k     Document Type: Article

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