/ Home
/ SUBMISSION

/ The BJOC
/ Diamond Open Access
/ Journal Statistics
/ Editorial Board
/ Community
/ Call for papers

/ Latest Articles
/ Most accessed
/ Thematic issues
/ Volumes
/ Authors

/ Alerts

/ TWITTER
/ LINKEDIN
/ Mastodon
/ RSS FEED

Empty search

Article Type

Publication Date Range

Search Tips

This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.

Search Examples

aromatic	the word “aromatic”
aromatic aldehyde	the word “aromatic” OR “aldehyde”
+aromatic +aldehyde	both words “aromatic” AND “aldehyde”
+aromatic -aldehyde	the word “aromatic” but NOT “aldehyde”
“aromatic aldehyde”	the exact phrase “aromatic aldehyde”
benz*	words which begin with “benz”, such as “benzene” or “benzyl”
benz*yl	words that begin with “benz” and end with “yl”, such as “benzyl” or “benzoyl”
benzyl~	words that are close to the word “benzyl”, such as “benzoyl” (i.e., fuzzy search)

BROWSE
Latest Articles
Most accessed
thematic issues
volumes
authors

BROWSE

Latest Articles Most Accessed Thematic Issues Volumes Authors

Author

2 article(s) from Reuter, Raphael

Profluorescent substrates for the screening of olefin metathesis catalysts

Raphael Reuter and
Thomas R. Ward

Beilstein J. Org. Chem. 2015, 11, 1886–1892, doi:10.3762/bjoc.11.203

PDF

Graphical Abstract

Figure 1: Catalysts 1–4 tested for the metathesis of profluorescent substrates.

Jump to Figure 1

Scheme 1: Two profluorescent substrates yielding fluorescent products upon ring-closing metathesis.

Jump to Scheme 1

Scheme 2: Synthesis of the two profluorescent substrates amenable to ring-closing metathesis.

Jump to Scheme 2

Figure 2: Fluorescence evolution resulting from closing metathesis of umbelliferone precursor 8 (λ_excitation ...

Jump to Figure 2

Figure 3: Fluorescence evolution resulting from closing metathesis of fluorescence–quencher substrate 5 (λ_exc...

Jump to Figure 3

Figure 4: Comparison of kinetics measured by HPLC a) and by a plate reader b) for the ring-closing metathesis...

Jump to Figure 4

Album

Supp Info

Full Research Paper

Published 12 Oct 2015

Full text

meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties

Raphael Reuter and
Hermann A. Wegner

Beilstein J. Org. Chem. 2012, 8, 877–883, doi:10.3762/bjoc.8.99

PDF

Graphical Abstract

Figure 1: para-Substituted bisazobiphenyls 1 investigated by Hecht (R¹, R² = H, Me, R³ = t-Bu) and by Woolley...

Jump to Figure 1

Figure 2: Synthetic strategy for the assembly of meta-substituted oligo-azobiphenyls 2.

Jump to Figure 2

Scheme 1: Synthesis of 2-nitro-4-tert-butyl-6-bromobenzoic acid (6).

Jump to Scheme 1

Scheme 2: Preparation of nitroso derivative 10.

Jump to Scheme 2

Scheme 3: Assembly of oligomer 2 by Suzuki cross-coupling and site-selective Mills reaction.

Jump to Scheme 3

Figure 3: Isomerization studies of compound 13 (a), 15 (b), 16 (c) and 2 (d) (Irradiation at 356 nm in CHCl₃)....

Jump to Figure 3

Figure 4: Comparison of the absorption as well as the photostationary state of compounds 13, 15, 16, 2.

Jump to Figure 4

Figure 5: Four different isomers of 2.

Jump to Figure 5

Album

Supp Info

Full Research Paper

Published 13 Jun 2012

Full text

Other Beilstein-Institut Open Science Activities

/ Help / Support & Contact / Alerts / Privacy Policy / Terms & Conditions / Impressum