Dechalcogenative allylic selenosulfide and disulfide rearrangements: Complementary methods for the formation of allylic sulfides in the absence of electrophiles. Scope, limitations, and application to the functionalization of unprotected peptides in aqueous media

Journal of the American Chemical Society

Volumn 129, Issue 33, 2007, Pages 10282-10294

  Crich, David ^a,b   Krishnamurthy, Venkataramanan ^a   Brebion, Franck ^a   Karatholuvhu, Maheswaran ^a,b   Subramanian, Venkataraman ^a,b   Hutton, Thomas K ^a  

^a UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

^b WAYNE STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; DERIVATIVES; METHANOL; PEPTIDES; SELENIUM COMPOUNDS; SOLUTIONS;

AQUEOUS MEDIA; DERIVATIZATION; ELECTROPHILES; ROOM TEMPERATURE;

SULFUR COMPOUNDS;

ACETONITRILE; ALLYL COMPOUND; ALLYL SULFIDE; DISULFIDE; METHANOL; SELENIUM DERIVATIVE;

AQUEOUS SOLUTION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; DERIVATIZATION; ROOM TEMPERATURE;

ALLYL COMPOUNDS; DISULFIDES; ORGANOSELENIUM COMPOUNDS; PEPTIDES; PHOSPHINES; SULFHYDRYL COMPOUNDS; SULFIDES;

EID: 34548155188     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja072969u     Document Type: Article

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