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(S)-10-(2-tert-butoxy-2-oxoethyl)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,10-diaza pentadecane-5-carboxylic acid

Base Information
  • Chemical Name:(S)-10-(2-tert-butoxy-2-oxoethyl)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,10-diaza pentadecane-5-carboxylic acid
  • CAS No.:151132-81-9
  • Molecular Formula:C33H44N2O8
  • Molecular Weight:596.721
  • Hs Code.:
(S)-10-(2-tert-butoxy-2-oxoethyl)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,10-diaza pentadecane-5-carboxylic acid

Synonyms:(S)-10-(2-tert-butoxy-2-oxoethyl)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,10-diaza pentadecane-5-carboxylic acid

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Chemical Property of (S)-10-(2-tert-butoxy-2-oxoethyl)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,10-diaza pentadecane-5-carboxylic acid
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Technology Process of (S)-10-(2-tert-butoxy-2-oxoethyl)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,10-diaza pentadecane-5-carboxylic acid

There total 2 articles about (S)-10-(2-tert-butoxy-2-oxoethyl)-1-(9H-fluoren-9-yl)-14,14-dimethyl-3,12-dioxo-2,13-dioxa-4,10-diaza pentadecane-5-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: dichloromethane / 0.5 h / 75 °C / Inert atmosphere
2: sodium tris(acetoxy)borohydride / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
With sodium tris(acetoxy)borohydride; In dichloromethane;
DOI:10.1021/bc900517x
Guidance literature:
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; solid phase reaction;
DOI:10.1016/j.bioorg.2009.05.003
upstream raw materials:

tert-butyl glyoxylate

Fmoc-Lys-OH

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