38478-72-7

Upstream product

• 89088-36-8 N,N-Dimethyl-L-alanyl-L-valine 
• 312583-30-5 (Z)-(3S,7S,10S)-10-Benzyl-2-oxa-6,9,12-triaza-tricyclo[13.2.2.0^3,7]nonadeca-1⁽¹⁸⁾,13,15⁽¹⁹⁾,16-tetraene-8,11-dione 
• 312583-27-0 (3S,7S,10S,14S)-10-Benzyl-8,11-dioxo-14-phenylselanyl-2-oxa-6,9,12-triaza-tricyclo[13.2.2.0^3,7]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-triene-6-carboxylic acid tert-butyl ester 
• 312583-26-9 (3S,7S,10S,14R)-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-carboxylic acid tert-butyl ester 
• 312583-28-1 (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-carboxylic acid tert-butyl ester 
• 312583-22-5 (2S,3S)-1-Benzyl-3-hydroxy-pyrrolidine-2-carboxylic acid {(S)-1-[(R)-2-(4-fluoro-3-nitro-phenyl)-2-hydroxy-ethylcarbamoyl]-2-phenyl-ethyl}-amide 
• 312583-23-6 (3S,7S,10S,14R)-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 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 856165-48-5 [(S)-1-((3S,7S,10S,14S)-10-Benzyl-8,11-dioxo-14-phenylselanyl-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]-carbamic acid tert-butyl ester 
• 856165-47-4 [(S)-1-((3S,7S,10S,14R)-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]-carbamic acid tert-butyl ester 
• 856165-49-6 [(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]-carbamic acid tert-butyl ester 
• 856165-43-0 {(S)-1-[(R)-2-(4-Fluoro-3-nitro-phenyl)-2-hydroxy-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester 
• 856165-51-0 (3S,7S,10S,14R)-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 
• 2812-31-9 N,N-dimethyl-L-alanine 

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.

The first total synthesis of mauritine-A

Total synthesis of mauritine-A is accomplished featuring a key cycloetherification reaction based on an intramolecular S(N)Ar reaction. (C) 2000 Elsevier Science Ltd.