Protecting Group Combinations for Solid-Phase Synthesis

12 PROTECTING GROUP COMBINATIONS FOR SOLID-PHASE SYNTHESIS 

RB Merrifield. Solid phase synthesis. III. An improved synthesis of bradykinin. Biochemistry 3, 1385, 1964. 

JM Schlatter, RH Mazur, O Goodmonson. Hydrogenation in solid phase peptide synthesis. I. Removal of product from the resin. Tetrahedron Lett 2851, 1977. 

CD Chang, J Meienhofer. Solid-phase synthesis using mild base cleavage of N -fluorenylmethoxycarbonylamino acids, exemplified by a synthesis of dihydrosomatostatin. Int J Pept Prot Res 11, 246, 1978. 

J Meienhofer, M Waki, EP Heimer, TJ Lambros, RC Makofske, C-D Chang. Solid phase synthesis without repetitive acidolysis. Int J Pept Prot Res 13, 35, 1979. 

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Sheppard RC, Williams BJ, A new protecting group combination for solid phase synthesis of protected peptides, J. Chem. Soc. Chem. Commun., 587-589, 1982. 

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