| Issue |
Section |
Title |
File |
| Vol 52, No 2 (2016) |
Article |
Homo and hetero glaser coupling involving acetylene derivatives of trifluoromethanesulfonamide |
|
| Vol 52, No 4 (2016) |
Review |
Synthesis and properties of N-(alkenylidene)trifluoromethanesulfonamides |
|
| Vol 52, No 7 (2016) |
Article |
Cyclization of trifluoro-N-(prop-2-yn-1-yl)methanesulfonamides to N-(hydroxymethyl)-1,2,3-triazoles |
|
| Vol 52, No 8 (2016) |
Article |
Reaction of N-phenyltriflamide with 1,2-dibromoethane and propargyl bromide. Unexpected cleavage of С–С and С–N bonds |
|
| Vol 52, No 12 (2016) |
Article |
Synthesis and bromination/dehydrobromination of N,N-diallyltrifluoromethanesulfonamide |
|
| Vol 53, No 4 (2017) |
Short Communications |
Reaction of trifluoro-N-(oxo-λ4-sulfanylidene)methanesulfonamide with pyrazolidin-3-ones |
|
| Vol 53, No 6 (2017) |
Article |
Unsaturated derivatives of trifluoromethanesulfonimide |
|
| Vol 53, No 6 (2017) |
Short Communications |
Oxidative iodination of N-propargyltriflamide |
|
| Vol 53, No 7 (2017) |
Article |
Oxidative trifluoroacetamidation of (1E,3E)-1,4-diphenylbuta-1,3-diene and 1,1,4,4-tetraphenylbuta-1,3-diene |
|
| Vol 53, No 10 (2017) |
Article |
N-allyl and N-propargyl trifluoromethanesulfonimides. Theoretical analysis |
|
| Vol 54, No 6 (2018) |
Article |
Reactions of N-Allyl- and N,N-Diallyltrifluoromethanesulfonamides with Carboxylic Acid Amides under Oxidizing Conditions |
|
| Vol 54, No 7 (2018) |
Short Communications |
Reactions of N-Allyl- and N-Propargyltriflimides with N,N′-Disubstituted Carbodiimides |
|
| Vol 55, No 2 (2019) |
Article |
Three-Component Reaction of Sulfonamides with Acetylene and Amines |
|
| Vol 55, No 3 (2019) |
Article |
Unusual Transformations of Highly Unsaturated Trifluoromethanesulfonamide Derivatives |
|
| Vol 55, No 3 (2019) |
Short Communication |
Reaction of N-Phenyltrifluoromethanesulfonamide with Carbodiimides |
|
| Vol 55, No 5 (2019) |
Short Communications |
Reaction of N,N′-Methylenebis(trifluoromethanesulfonamide) with Styrene under Oxidative Conditions |
|
