(2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine

Base Information

Chemical Name:(2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine
CAS No.:194936-43-1
Molecular Formula:C₃₄H₃₄N₂O₄S
Molecular Weight:566.721
Hs Code.:

Synonyms:(2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine

Suppliers and Price of (2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine

There total 1 articles about (2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine 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: 88.0%

: 2937-50-0
Allyl chloroformate

: 194936-42-0
(2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine

: 194936-43-1
(2S,4S)-N-allyloxycarbonyl-2-(3-allyloxycarbonylamino-1-propynyl)-4-tritylthiopyrrolidine

Guidance literature:: (2S,4S)-2-(3-allyloxycarbonylamino-1-propynyl)-N-t-butoxycarbonyl-4-tritylthiopyrrolidine; With trifluoroacetic acid; In dichloromethane; at 4 ℃; for 1h;

Allyl chloroformate; With triethylamine; In dichloromethane; at 4 ℃; for 1h;
DOI:10.7164/antibiotics.50.586