5- and 6-trifluoromethyldiazirinyl indoles were synthesized from corresponding bromoindole derivatives for the first time. They acted as mother skeletons for the comprehensive synthesis of various bioactive indole metabolites. These can be used in biological functional analysis as diazirine-based photoaffinity labels
Saccharin is one of the most common artificial sweeteners that has a bitter taste at high concentrat...
This paper reports a synthesis of novel diheteroarylethenes functionalized for coupling to biomolecu...
A versatile synthesis of diazirine-based photoreactive fatty acid analogues is reported. The key ste...
The 1,3,5-trisubstituted aryl diazirine(2) has been synthesised as a photoaffinity probe and has bee...
Alternative one-pot synthesis of 3-(trifluoromethyl)-3-phenyldiazirine derivatives from correspondin...
Based on the recent development of molecular biology, the investigation of biofunctional machinery a...
The previously unknown difluoromethyl diazirines and the previously neglected trifluoromethyl-alipha...
An improved synthesis of photoaffinity labeled, optically active retinal derivatives is presented. A...
Photoaffinity labeling is a quintessential technique in studying and analyzing the interaction betwe...
Target identification is a high-priority, albeit challenging, aspect of drug discovery. Diazirine-ba...
A simple and mild method was developed for the introduction of iodo-label on (3-trifluoromethyl) phe...
Includes bibliographical references (pages 44-45)A method for the synthesis of indole alkaloid-like ...
An intramolecular dearomatization of indole derivatives has been developed via an electron donor–acc...
The aim is to develop the methods for synthesis of the ATMFD-containing photoactivated reagents for ...
The use of organometallic reagents for functionalization of arenes and heterocycles has recently bee...
Saccharin is one of the most common artificial sweeteners that has a bitter taste at high concentrat...
This paper reports a synthesis of novel diheteroarylethenes functionalized for coupling to biomolecu...
A versatile synthesis of diazirine-based photoreactive fatty acid analogues is reported. The key ste...
The 1,3,5-trisubstituted aryl diazirine(2) has been synthesised as a photoaffinity probe and has bee...
Alternative one-pot synthesis of 3-(trifluoromethyl)-3-phenyldiazirine derivatives from correspondin...
Based on the recent development of molecular biology, the investigation of biofunctional machinery a...
The previously unknown difluoromethyl diazirines and the previously neglected trifluoromethyl-alipha...
An improved synthesis of photoaffinity labeled, optically active retinal derivatives is presented. A...
Photoaffinity labeling is a quintessential technique in studying and analyzing the interaction betwe...
Target identification is a high-priority, albeit challenging, aspect of drug discovery. Diazirine-ba...
A simple and mild method was developed for the introduction of iodo-label on (3-trifluoromethyl) phe...
Includes bibliographical references (pages 44-45)A method for the synthesis of indole alkaloid-like ...
An intramolecular dearomatization of indole derivatives has been developed via an electron donor–acc...
The aim is to develop the methods for synthesis of the ATMFD-containing photoactivated reagents for ...
The use of organometallic reagents for functionalization of arenes and heterocycles has recently bee...
Saccharin is one of the most common artificial sweeteners that has a bitter taste at high concentrat...
This paper reports a synthesis of novel diheteroarylethenes functionalized for coupling to biomolecu...
A versatile synthesis of diazirine-based photoreactive fatty acid analogues is reported. The key ste...