Orthohalogen substituents dramatically enhance hydrogen bonding of aromatic ureas in solution.
about
Tuning the nature and stability of self-assemblies formed by ester benzene 1,3,5-tricarboxamides: the crucial role played by the substituents.Time-dependent gel to gel transformation of a peptide based supramolecular gelator.Fluoroenesulphonamides: N-sulphonylurea isosteres showing nanomolar selective cancer-related transmembrane human carbonic anhydrase inhibition
P2860
Orthohalogen substituents dramatically enhance hydrogen bonding of aromatic ureas in solution.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh
2013年學術文章
@zh-hant
name
Orthohalogen substituents dram ...... of aromatic ureas in solution.
@en
Orthohalogen substituents dram ...... of aromatic ureas in solution.
@nl
type
label
Orthohalogen substituents dram ...... of aromatic ureas in solution.
@en
Orthohalogen substituents dram ...... of aromatic ureas in solution.
@nl
prefLabel
Orthohalogen substituents dram ...... of aromatic ureas in solution.
@en
Orthohalogen substituents dram ...... of aromatic ureas in solution.
@nl
P2093
P2860
P50
P356
P1476
Orthohalogen substituents dram ...... of aromatic ureas in solution
@en
P2093
Benjamin Isare
Benjamin Jouvelet
Ilaria Giannicchi
P2860
P304
P356
10.1039/C3CC47447J
P407
P577
2013-11-26T00:00:00Z