192370-37-9

Upstream product

• 82892-54-4 1-(benzyloxycarbonyl)-3-ethylimidazolium tetrafluoroborate 
• 192370-36-8 (Z)-5-(6-Azido-purin-9-yl)-3-(2-tert-butoxycarbonylamino-ethyl)-pent-3-enoic acid ethyl ester 
• 192370-32-4 (Z)-3-(2-Azido-ethyl)-5-(tert-butyl-diphenyl-silanyloxy)-pent-3-enoic acid ethyl ester 
• 192370-35-7 (Z)-3-(2-tert-Butoxycarbonylamino-ethyl)-5-(6-chloro-purin-9-yl)-pent-3-enoic acid ethyl ester 
• 192370-34-6 (Z)-3-(2-Azido-ethyl)-5-(6-chloro-purin-9-yl)-pent-3-enoic acid ethyl ester 
• 192370-24-4 (Z)-5-(tert-Butyl-diphenyl-silanyloxy)-3-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-pent-3-enoic acid ethyl ester 
• 192370-31-3 (Z)-5-(tert-Butyl-diphenyl-silanyloxy)-3-(2-hydroxy-ethyl)-pent-3-enoic acid ethyl ester 
• 192370-33-5 (Z)-3-(2-Azido-ethyl)-5-hydroxy-pent-3-enoic acid ethyl ester 
• 121353-11-5 (Z)-3-iodo-5-(tetrahydro-2H-pyran-2-yloxy)pent-2-en-1-ol 
• 51442-80-9 5-(tetrahydro-2H-pyran-2-yloxy)-2-pentyn-1-ol 

Relevant academic research and scientific papers

Synthesis of the monomeric building blocks of Z-olefinic (PNA) (Z-OPA) containing the bases Adenine and thymine

The synthesis of the Boc-protected Z-olefinic peptide nucleic acid analog (Z-OPA) monomers containing the base thymine II and Cbz-adenine 19 is described, Key step in the synthesis of the underlying carbon framework is a Pd(0)-catalyzed coupling of a viny