16938-11-7

Upstream product

• 3262-72-4 (S)-N-(tert-butoxycarbonyl)serine 
• 100-11-8 1-bromomethyl-4-nitro-benzene 

Downstream Products

• 106128-52-3 Boc-Ser(PO₃Ph₂)-ONb 
• 90236-61-6 (N^α-t-butoxycarbonyl)-O-(dibenzylphosphono)-L-serine p-nitrobenzyl ester 
• 118235-07-7 N^α-(t-butoxycarbonyl)-O-(di-t-butylphosphono)serine 4-nitrobenzyl ester 
• 84714-31-8 Boc-Ser(PO₃Et₂)-ONBzl 
• 133478-54-3 Boc-Ser(PO₃Me₂)-ONBzl 
• 109539-01-7 N^α-(t-butoxycarbonyl)-O-(dimethylphosphono)-L-serine 
• 133478-57-6 Boc-Ser(PO₃Bu^t2)-Leu-OBzl 
• 106111-03-9 Boc-Ser(PO₃Ph₂)-Leu-OBzl 
• 90013-46-0 Boc-Ser(PO₃Bzl₂)-Leu-OBzl 
• 105751-07-3 N^α-(t-butoxycarbonyl)-O-(diphenylphosphono)-L-serine 
• 90013-45-9 N^α-(t-butoxycarbonyl)-O-(dibenzylphosphono)-L-serine 

Relevant academic research and scientific papers

A NOVEL APPROACH TO PHOSPHOPEPTIDE SYNTHESIS-PREPARATION OF GLU-PSER-LEU

A synthesis of the phosphotripeptide Glu-PSer-Leu is reported via the stepwise incorporation of the protected phosphoamino acid Nα-tert-butoxycarbonyl-O-dibenzylphosphono-L-serine.

Total synthesis of the thiopeptide antibiotic amythiamicin D

The thiopeptide (or thiostrepton) antibiotics are a class of sulfur containing highly modified cyclic peptides with interesting biological properties, including reported activity against MRSA and malaria. Described herein is the total synthesis of the thi