Fmoc Chemistry
Fmoc Chemistry is a solid-phase peptide synthesis strategy that employs the 9-fluorenylmethoxycarbonyl (Fmoc) group as a base-labile protecting group for the alpha-amino function, enabling sequential assembly of peptides through selective deprotection and coupling cycles.
1.3K
Publications
61.5K
Citations
4.3K
Authors
1K
Institutions
Publications per year
2017–2026
172
1.3K
Recent advances in the trifluoromethylation methodology and new CF3-containing drugs
Wei Zhu, Jiang Wang, Shuni Wang et al. · Journal of Fluorine Chemistry · 2014 · 488 citations
1–5 of 1.3K
4.3K
35
h-index
21
h-index
18
h-index
Leibniz-Forschungsinstitut für Molekulare Pharmakologie, Germany
17 publications · 902 citations
17
h-index
15
h-index
1–5 of 4.3K
1K
Universitat de Barcelona
Barcelona, Spain
32 h-index
172 publications
8.3K citations

Centre National de la Recherche Scientifique
Paris, France
29 h-index
225 publications
10.5K citations

University of Minnesota
Minneapolis, United States
24 h-index
101 publications
5K citations
Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine
Madrid, Spain
22 h-index
67 publications
2.6K citations

University of KwaZulu-Natal
Durban, South Africa
20 h-index
74 publications
3.2K citations

The University of Melbourne
Melbourne, Australia
17 h-index
75 publications
3.2K citations
Scripps Research Institute
San Diego, United States
16 h-index
64 publications
7.1K citations
ETH Zurich
Zurich, Switzerland
16 h-index
54 publications
2.5K citations
1–8 of 1K
154 publications · 6.5K citations
42
h-index
JOC · 110 publications · 5.5K citations
42
h-index
77 publications · 5.2K citations
36
h-index
OL · 94 publications · 4.4K citations
36
h-index
JACS · 34 publications · 5K citations
33
h-index
1–5