1403825-72-8Relevant articles and documents
Acid-labile cys-protecting groups for the Fmoc/tBu strategy: Filling the gap
Góngora-Benítez, Miriam,Mendive-Tapia, Lorena,Ramos-Tomillero, Iván,Breman, Arjen C.,Tulla-Puche, Judit,Albericio, Fernando
, p. 5472 - 5475 (2012)
To address the existing gap in the current set of acid-labile Cys-protecting groups for the Fmoc/tBu strategy, diverse Fmoc-Cys(PG)-OH derivatives were prepared and incorporated into a model tripeptide to study their stability against TFA. S-Dpm proved to be compatible with the commonly used S-Trt group and was applied for the regioselecive construction of disulfide bonds.
Acid-labile cys-protecting groups for the Fmoc/tBu strategy: Filling the gap
Gongora-Benitez, Miriam,Mendive-Tapia, Lorena,Ramos-Tomillero, Ivan,Breman, Arjen C.,Tulla-Puche, Judit,Albericio, Fernando
supporting information, p. 5472 - 5475,4 (2012/12/12)
To address the existing gap in the current set of acid-labile Cys-protecting groups for the Fmoc/tBu strategy, diverse Fmoc-Cys(PG)-OH derivatives were prepared and incorporated into a model tripeptide to study their stability against TFA. S-Dpm proved to be compatible with the commonly used S-Trt group and was applied for the regioselecive construction of disulfide bonds.