/ 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

1 article(s) from Tripoteau, Fabien

Boron-substituted 1,3-dienes and heterodienes as key elements in multicomponent processes

Ludovic Eberlin,
Fabien Tripoteau,
François Carreaux,
Andrew Whiting and
Bertrand Carboni

Beilstein J. Org. Chem. 2014, 10, 237–250, doi:10.3762/bjoc.10.19

PDF

Graphical Abstract

Scheme 1: 1-Boron-substituted 1,3-diene in a tandem cycloaddition [4 + 2]/allylboration sequence.

Jump to Scheme 1

Scheme 2: Lewis acid catalyst in the tandem cycloaddition [4 + 2]/allylboration sequence.

Jump to Scheme 2

Scheme 3: Synthesis of an advanced precursor of clerodin.

Jump to Scheme 3

Scheme 4: Intramolecular Diels–Alder/allylboration sequence.

Jump to Scheme 4

Scheme 5: Diastereoselective Diels–Alder reaction with N-phenylmaleimide and 4-phenyltriazoline-3,5-dione.

Jump to Scheme 5

Scheme 6: Asymmetric synthesis of a α-hydroxyalkylcyclohexane.

Jump to Scheme 6

Scheme 7: Tandem [4 + 2]-cycloaddition/allylboration of 3-silyloxy- and 4-alkoxy-dienyl boronates.

Jump to Scheme 7

Scheme 8: Metal-mediated cycloisomerization/Diels–Alder reaction/allylboration sequence.

Jump to Scheme 8

Scheme 9: Cobalt-catalyzed Diels–Alder/allylboration sequence.

Jump to Scheme 9

Scheme 10: A two-step reaction sequence for the synthesis of tetrahydronaphthalenes 12.

Jump to Scheme 10

Scheme 11: Tandem sequence based on the Petasis borono–Mannich reaction as first key step.

Jump to Scheme 11

Scheme 12: One-pot tandem dimerization/allylboration reaction of 1,3-diene-2-boronate.

Jump to Scheme 12

Scheme 13: Tandem Diels–Alder/cross-coupling reactions of trifluoroborates 15.

Jump to Scheme 13

Scheme 14: Diels–Alder/cross-coupling reactions of 16.

Jump to Scheme 14

Scheme 15: Metal catalyzed tandem Diels–Alder/hydrolysis reactions.

Jump to Scheme 15

Scheme 16: Synthesis of anti-1,5-diols 18 by triple aldehyde addition.

Jump to Scheme 16

Scheme 17: Catalytic enantioselective three-component hetero-[4 + 2]-cycloaddition/allylboration sequence.

Jump to Scheme 17

Scheme 18: Synthesis of natural products using the catalytic enantioselective HDA/allylboration sequence.

Jump to Scheme 18

Scheme 19: Total synthesis of a thiomarinol derivative.

Jump to Scheme 19

Scheme 20: Synthesis of an advanced intermediate 27 for the east fragment of palmerolide A.

Jump to Scheme 20

Scheme 21: Bicyclic piperidines from tandem aza-[4 + 2]-cycloaddition/allylboration.

Jump to Scheme 21

Scheme 22: Hydrogenolysis reactions of hydrazinopiperidines.

Jump to Scheme 22

Scheme 23: Tandem aza-[4 + 2]-cycloaddition/allylboration/retrosulfinyl-ene sequence.

Jump to Scheme 23

Scheme 24: Boronated heterodendralene 32 in [4 + 2]-cycloadditions.

Jump to Scheme 24

Scheme 25: Synthesis of tricyclic imides derivatives.

Jump to Scheme 25

Scheme 26: Synthesis of 37 via a HDA/allylboration/DA sequence.

Jump to Scheme 26

Scheme 27: Diels–Alder/allylboration sequence.

Jump to Scheme 27

Album

Review

Published 22 Jan 2014

Full text

Other Beilstein-Institut Open Science Activities

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