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July 28, 2006
Allylic disulfide rearrangement and desulfurization: mild, electrophile-free thioether formation from thiols
David Crich, Franck Brebion, Venkataramanan Krishnamurthy
Journal of the American Chemical Society
|
February 24, 2006
Allylic selenosulfide rearrangement: a method for chemical ligation to cysteine and other thiols
David Crich, Venkataramanan Krishnamurthy, Thomas K Hutton
Accounts of Chemical Research
|
May 11, 2007
Catalysis of stannane-mediated radical chain reactions by benzeneselenol
David Crich, Daniel Grant, Venkataramanan Krishnamurthy, et al.
Journal of the American Chemical Society
|
July 28, 2007
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
David Crich, Venkataramanan Krishnamurthy, Franck Brebion, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Organic Letters
|
July 28, 2006
Allylic disulfide rearrangement and desulfurization: mild, electrophile-free thioether formation from thiols
David Crich, Franck Brebion, Venkataramanan Krishnamurthy
Journal of the American Chemical Society
|
February 24, 2006
Allylic selenosulfide rearrangement: a method for chemical ligation to cysteine and other thiols
David Crich, Venkataramanan Krishnamurthy, Thomas K Hutton
Accounts of Chemical Research
|
May 11, 2007
Catalysis of stannane-mediated radical chain reactions by benzeneselenol
David Crich, Daniel Grant, Venkataramanan Krishnamurthy, et al.
Journal of the American Chemical Society
|
July 28, 2007
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
David Crich, Venkataramanan Krishnamurthy, Franck Brebion, et al.
Page
of 1