Published TCIMAIL newest issue No.200 | Product Document Searching Made Easy by 2D Code! | TCI Life Science News December 2025 | [Product Highlights] Cell Culture-Ready Antibiotic... | Various analytical charts can be searched on each product detail page and Product Document Search (The kinds of analytical charts differ by product)
Maximum quantity allowed is 999
Please select the quantity
Sulfonyl Azide Useful for Introduction of Azido and Diazo Groups
2,4,6-Triisopropylbenzenesulfonyl azide (1) can be used as an electrophilic azidation agent or a diazotizing agent.1,2) When 1 reacts with a suitable base on a substrate containing a carbonyl group, an azido or diazo group can be introduced at the α-position. Recently, decarboxylative azidation reactions using visible light redox catalysts have also been reported.3) For example, using proline derivatives as substrates yield 2-azidopyrrolidine derivatives.

Related Products
- T3434
- 2,4,6-Triisopropylbenzenesulfonyl Azide (wetted with ca. 10% Water)
- T0054
- Tetrabutylammonium Bromide
- C0860
- 18-Crown 6-Ether
- P2844
- Potassium Hydroxide (Powder)
- R0039
- Rhodamine 6G
References
- 1) A General Method for Making Peptide Therapeutics Resistant to Serine Protease Degradation: Application to Dipeptidyl Peptidase IV Substrates
- 2) Symmetry in retrosynthetic analysis:(±)-pentalenolactone e methyl ester
- 3) Photoinduced decarboxylative azidation of cyclic amino acids