856165-45-2

Upstream product

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 312583-24-7 (2S,3S)-1-Benzyl-3-hydroxy-pyrrolidine-2-carboxylic acid {(S)-1-[(S)-2-(4-fluoro-3-nitro-phenyl)-2-hydroxy-ethylcarbamoyl]-2-phenyl-ethyl}-amide 
• 312583-25-8 (3S,7S,10S,14S)-6,10-Dibenzyl-14-hydroxy-2-oxa-6,9,12-triaza-tricyclo[13.2.2.0^3,7]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-triene-8,11-dione 
• 856165-44-1 [(S)-1-((3S,7S,10S,14S)-10-Benzyl-14-hydroxy-8,11-dioxo-2-oxa-6,9,12-triaza-tricyclo[13.2.2.0^3,7]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-triene-6-carbonyl)-2-methyl-propyl]-methyl-carbamic acid tert-butyl ester 
• 856165-52-1 {(S)-1-[(S)-2-(4-Fluoro-3-nitro-phenyl)-2-hydroxy-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester 
• 856165-42-9 (3S,7S,10S,14S)-10-Benzyl-14-hydroxy-2-oxa-6,9,12-triaza-tricyclo[13.2.2.0^3,7]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-triene-8,11-dione 
• 1666-13-3 diphenyl diselenide 

Downstream Products

• 856165-46-3 [(S)-1-((Z)-(3S,7S,10S)-10-Benzyl-8,11-dioxo-2-oxa-6,9,12-triaza-tricyclo[13.2.2.0^3,7]nonadeca-1⁽¹⁸⁾,13,15⁽¹⁹⁾,16-tetraene-6-carbonyl)-2-methyl-propyl]-methyl-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Total synthesis of mauritines A, B, C, and F: Cyclopeptide alkaloids with a 14-membered paracyclophane unit

A unified strategy for the synthesis of mauritines A (5), B (6), C (7), and F (10) has been developed based on a key intramolecular nucleophilic aromatic substitution reaction (SNAr) for the formation of the strained 14-membered paracyclophane.