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pro vyhledávání: '"Rameshwor Acharya"'
Autor:
Kyle N. Hearn, Trent D. Ashton, Rameshwor Acharya, Zikai Feng, Nuri Gueven, Frederick M. Pfeffer
Publikováno v:
Cells, Vol 10, Iss 6, p 1505 (2021)
Methodology to access fluorescent 3-amido-1,8-naphthalimides using direct Buchwald–Hartwig amidation is described. The protocol was successfully used to couple a number of substrates (including an alkylamide, an arylamide, a lactam and a carbamate)
Externí odkaz:
https://doaj.org/article/f6951505ff2141cf9075d7a1f91dcb72
Autor:
Rameshwor Acharya, Zikai Feng, Nuri Gueven, Rosalind P. Cox, Trent D. Ashton, Frederick M. Pfeffer, Elley E. Rudebeck, Toby D. M. Bell
Publikováno v:
Chemical Communications. 56:6866-6869
An efficient and functional group tolerant route to access hydroxy 1,8-naphthalimides has been used to synthesise a range of mono- and disubstituted hydroxy-1,8-naphthalimides with fluorescence emissions covering the visible spectrum. The dialkoxy su
Autor:
Nuri Gueven, Rameshwor Acharya, Frederick M. Pfeffer, Kyle N Hearn, Trent D. Ashton, Zikai Feng
Publikováno v:
Cells
Volume 10
Issue 6
Cells, Vol 10, Iss 1505, p 1505 (2021)
Volume 10
Issue 6
Cells, Vol 10, Iss 1505, p 1505 (2021)
Methodology to access fluorescent 3-amido-1,8-naphthalimides using direct Buchwald–Hartwig amidation is described. The protocol was successfully used to couple a number of substrates (including an alkylamide, an arylamide, a lactam and a carbamate)