/ Home
/ SUBMISSION

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

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

/ E-Alerts

/ BlueSky
/ 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
Featured Collections
volumes
authors

BROWSE

Latest Articles Most Accessed Thematic Issues Featured Collections Volumes Authors

Author

2 article(s) from Lin, Bin

Pathway economy in cyclization of 1,n-enynes

Hezhen Han,
Wenjie Mao,
Bin Lin,
Maosheng Cheng,
Lu Yang and
Yongxiang Liu

Beilstein J. Org. Chem. 2025, 21, 2260–2282, doi:10.3762/bjoc.21.173

PDF

Graphical Abstract

Scheme 1: Economical synthesis and pathway economy.

Jump to Scheme 1

Scheme 2: Au(I)-catalyzed cascade cyclization paths of 1,5-enynes.

Jump to Scheme 2

Scheme 3: Au(I)-catalyzed cyclization paths of 1,7-enynes.

Jump to Scheme 3

Scheme 4: I₂/TBHP-mediated radical cycloisomerization paths of 1,n-enyne.

Jump to Scheme 4

Scheme 5: Au(I)-catalyzed cycloisomerization paths of 3-allyloxy-1,6-diynes.

Jump to Scheme 5

Scheme 6: Pd(II)-catalyzed cycloisomerization paths of 2-alkynylbenzoate-cyclohexadienone.

Jump to Scheme 6

Scheme 7: Stereoselective cyclization of 1,5-enynes.

Jump to Scheme 7

Scheme 8: Substituent-controlled cycloisomerization of propargyl vinyl ethers.

Jump to Scheme 8

Scheme 9: Au(I)-catalyzed pathway-controlled domino cyclization of 1,2-diphenylethynes.

Jump to Scheme 9

Scheme 10: Au(I)-catalyzed tandem cyclo-isomerization of tryptamine-N-ethynylpropiolamide.

Jump to Scheme 10

Scheme 11: Au(I)-catalyzed tunable cyclization of 1,6-cyclohexenylalkyne.

Jump to Scheme 11

Scheme 12: Substituent-controlled 7-exo- and 8-endo-dig-selective cyclization of 2-propargylaminobiphenyl deri...

Jump to Scheme 12

Scheme 13: BiCl₃-catalyzed cycloisomerization of tryptamine-ynamide derivatives.

Jump to Scheme 13

Scheme 14: Au(I)-mediated substituent-controlled cycloisomerization of 1,6-enynes.

Jump to Scheme 14

Scheme 15: Ligand-controlled regioselective cyclization of 1,6-enynes.

Jump to Scheme 15

Scheme 16: Ligand-dependent cycloisomerization of 1,7-enyne esters.

Jump to Scheme 16

Scheme 17: Ligand-controlled cycloisomerization of 1,5-enynes.

Jump to Scheme 17

Scheme 18: Ligand-controlled cyclization strategy of alkynylamide tethered alkylidenecyclopropanes.

Jump to Scheme 18

Scheme 19: Ag(I)-mediated pathway-controlled cycloisomerization of tryptamine-ynamides.

Jump to Scheme 19

Scheme 20: Gold-catalyzed cycloisomerization of indoles with alkynes.

Jump to Scheme 20

Scheme 21: Catalyst-dependent cycloisomerization of dienol silyl ethers.

Jump to Scheme 21

Scheme 22: Cycloisomerization of aromatic enynes governed by catalyst.

Jump to Scheme 22

Scheme 23: Catalyst-dependent 1,2-migration in cyclization of 1-(indol-2-yl)-3-alkyn-1-ols.

Jump to Scheme 23

Scheme 24: Gold-catalyzed cycloisomerization of N-propargyl-N-vinyl sulfonamides.

Jump to Scheme 24

Scheme 25: Gold(I)-mediated enantioselective cycloisomerizations of ortho-(alkynyl)styrenes.

Jump to Scheme 25

Scheme 26: Catalyst-controlled intramolecular cyclization of 1,7-enynes.

Jump to Scheme 26

Scheme 27: Brønsted acid-catalyzed cycloisomerizations of tryptamine ynamides.

Jump to Scheme 27

Scheme 28: Catalyst-controlled cyclization of indolyl homopropargyl amides.

Jump to Scheme 28

Scheme 29: Angle strain-dominated 6-endo-trig cyclization of propargyl vinyl ethers.

Jump to Scheme 29

Scheme 30: Angle strain-controlled cycloisomerization of alkyn-tethered indoles.

Jump to Scheme 30

Scheme 31: Geometrical isomeration-dependent cycloisomerization of 1,3-dien-5-ynes.

Jump to Scheme 31

Scheme 32: Temperature-controlled cyclization of 1,7-enynes.

Jump to Scheme 32

Scheme 33: Cycloisomerizations of n-(o-ethynylaryl)acrylamides through temperature modulation.

Jump to Scheme 33

Scheme 34: Temperature-controlled boracyclization of biphenyl-embedded 1,3,5-trien-7-ynes.

Jump to Scheme 34

Album

Review

Published 27 Oct 2025

Full text

Towards racemizable chiral organogelators

Jian Bin Lin,
Debarshi Dasgupta,
Seda Cantekin and
Albertus P. H. J. Schenning

Beilstein J. Org. Chem. 2010, 6, 960–965, doi:10.3762/bjoc.6.107

PDF

Graphical Abstract

Scheme 1: Synthesis of R-3 and S-3.

Jump to Scheme 1

Figure 1: Concentration-dependent ¹H NMR spectra of R-3 in chloroform (CDCl₃). The red colours indicate the h...

Jump to Figure 1

Figure 2: a) R-3 gel in octane (5 mM); b) octane solution containing a mixture of R-3 (2.5 mM) and S-3 (2.5 m...

Jump to Figure 2

Figure 3: a) Concentration-dependent ¹H NMR spectra of R-3 in cyclohexane-d₁₂ and b) the shift of N–H signal ...

Jump to Figure 3

Figure 4: The evolution of ln(ee × 100) for the racemization of R-3 (1 mM) in the presence of 1 equivalent of...

Jump to Figure 4

Album

Letter

Published 06 Oct 2010

Full text

Other Beilstein-Institut Open Science Activities

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