/ 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 Nagorny, Pavel

New approaches to organocatalysis based on C–H and C–X bonding for electrophilic substrate activation

Pavel Nagorny and
Zhankui Sun

Beilstein J. Org. Chem. 2016, 12, 2834–2848, doi:10.3762/bjoc.12.283

PDF

Graphical Abstract

Figure 1: Electrophile Activation by Hydrogen Bond Donors [1-16].

Jump to Figure 1

Figure 2: Early examples of C–H hydrogen bonds and their recent use in supramolecular chemistry [18,19,32-34].

Jump to Figure 2

Scheme 1: Design of 1,2,3-triazole-based catalysts for trityl group transfer through chloride anion binding b...

Jump to Scheme 1

Scheme 2: Examples of chiral triazole-based catalysts for anion activation designed by Mancheno and co-worker...

Jump to Scheme 2

Scheme 3: Application of chiral triazole-based catalysts L3 and L4 for counterion activation of pyridinium, q...

Jump to Scheme 3

Scheme 4: Ammonium salt anion binding via C–H hydrogen bonds in solid state [40-45,50,51].

Jump to Scheme 4

Scheme 5: Early examples of ammonium salts being used for electrophilic activation of imines in aza-Diels–Ald...

Jump to Scheme 5

Scheme 6: Ammonium salts as hydrogen bond-donor catalysts by Bibal and co-workers [53,54].

Jump to Scheme 6

Scheme 7: Tetraalkylammonium catalyst (L6)-catalyzed dearomatization of isoquinolinium salts [50].

Jump to Scheme 7

Scheme 8: Tetraalkylammonium catalyst L6 complexation to halogen-containing substrates [51].

Jump to Scheme 8

Scheme 9: Tetraalkylammonium-catalyzed aza-Diels–Alder reaction by Maruoka and co-workers [52].

Jump to Scheme 9

Scheme 10: (A) Alkylpyridinium catalysts L13-catalyzed reaction of 1-isochroman and silyl ketene acetals by Be...

Jump to Scheme 10

Scheme 11: Mixed N–H/C–H two hydrogen bond donors L14 and L15 as organocatalysts for ROP of lactide by Bibal a...

Jump to Scheme 11

Scheme 12: Examples of stable complexes based on halogen bonding [68,69].

Jump to Scheme 12

Scheme 13: Interaction between (−)-sparteine hydrobromide and (S)-1,2-dibromohexafluoropropane in the cocrysta...

Jump to Scheme 13

Scheme 14: Iodine-catalyzed reactions that are computationally proposed to proceed through halogen bond to car...

Jump to Scheme 14

Scheme 15: Transfer hydrogenation of phenylquinolines catalyzed by haloperfluoroalkanes by Bolm and co-workers ...

Jump to Scheme 15

Scheme 16: Halogen bond activation of benzhydryl bromides by Huber and co-workers [82].

Jump to Scheme 16

Scheme 17: Halogen bond-donor-catalyzed addition to oxocarbenium ions by Huber and co-workers [89].

Jump to Scheme 17

Scheme 18: Halogen bond-donor activation of α,β-unsaturated carbonyl compounds in the [2 + 4] cycloaddition re...

Jump to Scheme 18

Scheme 19: Halogen bond donor activation of imines in the [2 + 4] cycloaddition reaction of imine and Danishef...

Jump to Scheme 19

Scheme 20: Transfer hydrogenation catalyzed by a chiral halogen bond donor by Tan and co-workers [91].

Jump to Scheme 20

Scheme 21: Allylation of benzylic alcohols by Takemoto and co-workers [92].

Jump to Scheme 21

Scheme 22: NIS induced semipinacol rearrangement via C–X bond cleavage [93].

Jump to Scheme 22

Album

Review

Published 23 Dec 2016

Full text

Other Beilstein-Institut Open Science Activities

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