/ 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

3 article(s) from Wang, Rui

Site-selective reactions mediated by molecular containers

Rui Wang and
Yang Yu

Beilstein J. Org. Chem. 2022, 18, 309–324, doi:10.3762/bjoc.18.35

PDF

Graphical Abstract

Figure 1: Site-selective Diels–Alder reaction of anthracene and phthalimide mediated by aqueous organopalladi...

Jump to Figure 1

Figure 2: Site-selective Diels–Alder and [2 + 2]-photoaddition reactions between naphthalene and phthalimide ...

Jump to Figure 2

Figure 3: Cage host A-mediated selective 1,4-radical addition of o-quinone 10.

Jump to Figure 3

Figure 4: Cyclodextrin-mediated site-selective reductions.

Jump to Figure 4

Figure 5: Selective reduction of an α,ω-diazide compound mediated by water-soluble cavitand D.

Jump to Figure 5

Figure 6: Selective radical reduction of α,ω-dihalides mediated by water-soluble cavitands E and F.

Jump to Figure 6

Figure 7: Site-selective hydrogenation of polyenols mediated by supramolecular encapsulated rhodium catalyst.

Jump to Figure 7

Figure 8: Site-selective oxidation of steroids using cyclodextrin as the anchoring template.

Jump to Figure 8

Figure 9: Site-selective oxidations of linear diterpenoids with the help of cage host A.

Jump to Figure 9

Figure 10: Site-selective monoepoxidation of α,ω-dienes mediated by the water-soluble cavitand host E.

Jump to Figure 10

Figure 11: Site-selective ring-opening reaction of epoxides mediated by cavitand I with an inwardly directed c...

Jump to Figure 11

Figure 12: Site-selective nucleophilic substitution reaction of allylic chlorides mediated by cage host J.

Jump to Figure 12

Figure 13: Site-selective monohydrolysis of α,ω-difunctional compounds using deep water-soluble cavitands.

Jump to Figure 13

Album

Review

Published 14 Mar 2022

Full text

Water-soluble host–guest complexes between fullerenes and a sugar-functionalized tribenzotriquinacene assembling to microspheres

Si-Yuan Liu,
Xin-Rui Wang,
Man-Ping Li,
Wen-Rong Xu and
Dietmar Kuck

Beilstein J. Org. Chem. 2020, 16, 2551–2561, doi:10.3762/bjoc.16.207

PDF

Graphical Abstract

Figure 1: Selected TBTQ derivatives 1–5 that bind fullerenes in host–guest complexes.

Jump to Figure 1

Scheme 1: Synthetic route to TBTQ-(OG)₆.

Jump to Scheme 1

Figure 2: Fluorescence spectra of TBTQ-(OG)₆ (5.0 × 10⁻⁶ M) with varying concentrations of (a) C₆₀ and (b) C₇₀...

Jump to Figure 2

Figure 3: Absorption spectra of (a) TBTQ-(OG)₆ [Graphic 2] C₆₀ [TBTQ-(OG)₆: 50 μM; C₆₀: 50 μM] and (b) TBTQ-(OG)₆ C₇₀ [...

Jump to Figure 3

Figure 4: Absorption spectra of (a) TBTQ-(OG)₆ [Graphic 2] C₆₀ [TBTQ-(OG)₆: 50 μM; C₆₀: 50 μM] and (b) TBTQ-(OG)₆ C₇₀ [...

Jump to Figure 4

Figure 5: Raman spectra of TBTQ-G₆, C₆₀ and TBTQ-G₆ [Graphic 2] C₆₀. Sample solutions of TBTQ-(OG)₆ (50 μM) and TBTQ-(OG)...

Jump to Figure 5

Figure 6: Molecular model of the complex TBTQ-(OG)₆ [Graphic 2] C₆₀ in water, as generated by DFT calculations. (a) Side...

Jump to Figure 6

Figure 7: SEM images of (a) C₆₀; (b) TBTQ-(OG)₆; (c) and (d) TBTQ-(OG)₆ [Graphic 2] C₆₀ (C₆₀: 1.4 mM; TBTQ-(OG)₆: 1.4 mM...

Jump to Figure 7

Album

Supp Info

Full Research Paper

Published 14 Oct 2020

Full text

Synthesis of new tricyclic 5,6-dihydro-4H-benzo[b][1,2,4]triazolo[1,5-d][1,4]diazepine derivatives by [3⁺ + 2]-cycloaddition/rearrangement reactions

Lin-bo Luan,
Zi-jie Song,
Zhi-ming Li and
Quan-rui Wang

Beilstein J. Org. Chem. 2018, 14, 1826–1833, doi:10.3762/bjoc.14.155

PDF

Graphical Abstract

Figure 1: Examples of marketed pharmaceutical 1,2,4-triazolobenzodiazepines.

Jump to Figure 1

Scheme 1: Preparation of N-acylated 2,3-dihydro-4(1H)-quinolones 6.

Jump to Scheme 1

Scheme 2: Synthesis of α-acetoxyazo compounds 8a–g. Reaction conditions: for synthesis of 8a: 7a (10.42 mmol)...

Jump to Scheme 2

Scheme 3: Synthesis of tricyclic benzo[b][1,2,4]triazolo[1,5-d][1,4]diazepinium salts 10. Reaction conditions...

Jump to Scheme 3

Scheme 4: Synthesis of N(1)-unsubstituted benzo[b][1,2,4]triazolo[1,5-d][1,4]diazepines 13. Reaction conditio...

Jump to Scheme 4

Scheme 5: Mechanistic rationale for the [3⁺ + 2]-cycloaddition/rearrangement reaction.

Jump to Scheme 5

Figure 2: Crystal structure of salt 10k. The displacement ellipsoids are drawn at the 30% probability level.

Jump to Figure 2

Figure 3: Crystal structure of the free base 13e. The displacement ellipsoids are drawn at the 30% probabilit...

Jump to Figure 3

Album

Supp Info

Full Research Paper

Published 18 Jul 2018

Full text

Other Beilstein-Institut Open Science Activities

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

Site-selective reactions mediated by molecular containers

Water-soluble host–guest complexes between fullerenes and a sugar-functionalized tribenzotriquinacene assembling to microspheres

Synthesis of new tricyclic 5,6-dihydro-4H-benzo[b][1,2,4]triazolo[1,5-d][1,4]diazepine derivatives by [3+ + 2]-cycloaddition/rearrangement reactions

Synthesis of new tricyclic 5,6-dihydro-4H-benzo[b][1,2,4]triazolo[1,5-d][1,4]diazepine derivatives by [3⁺ + 2]-cycloaddition/rearrangement reactions