Franck Brebion

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. · Journal of the American Chemical Society · 2007 · 57 citations · Full text

Sulfide Transfer, Engineering, Biochemistry +15

Highly Diastereoselective Conjugate Addition to Alkylidene Bis(Sulfoxides): Asymmetric Synthesis of (+)‐<i>erythro</i>‐Roccellic Acid

Franck Brebion, Bénédicte Delouvrié, Francisco Nájera et al. · Angewandte Chemie International Edition · 2003 · 42 citations

Sigmatropic Rearrangements as Tools for Amino Acid and Peptide Modification:  Application of the Allylic Sulfur Ylide Rearrangement to the Preparation of Neoglycoconjugates and Other Conjugates

David Crich, Yekui Zou, Franck Brebion · The Journal of Organic Chemistry · 2006 · 36 citations · Full text

Bioorganic Chemistry, Engineering, Peptide Engineering +16

Enantioselective alkene radical cations reactions

David Crich, Michio Shirai, Franck Brebion et al. · Tetrahedron · 2006 · 34 citations

Alkene Metathesis, Organic Chemistry, Chemistry +2

Allylic Disulfide Rearrangement and Desulfurization:  Mild, Electrophile-Free Thioether Formation from Thiols

David Crich, Franck Brebion, Venkataramanan Krishnamurthy · Organic Letters · 2006 · 34 citations

Room Temperature, Engineering, 2-Benzothiazolyl Disulfides React +13