N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester

Base Information

Chemical Name:N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester
CAS No.:1053208-90-4
Molecular Formula:C₂₈H₃₃IN₂O₆
Molecular Weight:620.484
Hs Code.:

Synonyms:N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester

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Technology Process of N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester

There total 1 articles about N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester 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:

Reference yield: 89.0%

: 144599-94-0
N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-L-tryptophan benzyl ester

: 1053208-90-4
N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester

Guidance literature:: N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-L-tryptophan benzyl ester; With mercury(II) trifluoroacetate; In dichloromethane; Inert atmosphere;

With iodine; regioselective reaction; Inert atmosphere;
DOI:10.1021/ol8015513

Reference yield: 62.0%

: 1053208-90-4
N-tert-butoxycarbonyl-1-tert-butoxycarbonyl-2-iodo-L-tryptophan benzyl ester

: 1053208-98-2
(S)-1,8-bis-(tert-butoxycarbonyl)-1,2,3,8-tetrahydro-pyrrolo[2,3-b]indole-2-carboxylic acid methyl ester

Guidance literature:: With potassium phosphate; copper(l) iodide; N,N`-dimethylethylenediamine; In toluene; at 110 ℃; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ol8015513