X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
chemistry, multidisciplinary (6) 6
index medicus (6) 6
catalysis (5) 5
analysis (3) 3
chemical properties (3) 3
chemistry, organic (3) 3
directed tosyl chemistry (3) 3
living cells (3) 3
nickel (3) 3
activity-based probes (2) 2
alkaloids (2) 2
animals (2) 2
arylation (2) 2
arylboronic acids (2) 2
bond functionalization (2) 2
boronic acids (2) 2
c-h arylation (2) 2
carbon compounds (2) 2
catalyzed direct arylation (2) 2
chemical synthesis (2) 2
cross-coupling (2) 2
cysteine proteases (2) 2
derivatives (2) 2
deubiquitinating enzyme (2) 2
heterocycles (2) 2
humans (2) 2
in-vivo (2) 2
natural-products (2) 2
nickel - chemistry (2) 2
nickel catalysis (2) 2
palladium (2) 2
protease activity (2) 2
proteins - analysis (2) 2
regioselective reactions (2) 2
rhodium carbenoids (2) 2
ring transformation (2) 2
small-molecule (2) 2
strategy (2) 2
target identification (2) 2
4+2 cycloaddition (1) 1
4-aminopyridine - analogs & derivatives (1) 1
4-aminopyridine - chemistry (1) 1
a549 cells (1) 1
access (1) 1
acid (1) 1
acids (1) 1
acyl (1) 1
acylation (1) 1
alkaloids - chemical synthesis (1) 1
alkaloids - chemistry (1) 1
alkylation (1) 1
amythiamicin-d (1) 1
anhydrides (1) 1
anti-bacterial agents - chemical synthesis (1) 1
anti-bacterial agents - chemistry (1) 1
antibiotics (1) 1
apparatus therefor (1) 1
arenes (1) 1
azoles (1) 1
azoles - chemical synthesis (1) 1
azoles - chemistry (1) 1
benzoic-acids (1) 1
biocompatibility (1) 1
biological products - chemical synthesis (1) 1
biological products - chemistry (1) 1
bond arylation (1) 1
brain chemistry (1) 1
c-h borylation (1) 1
c-h coupling (1) 1
c-h functionalization (1) 1
cancer (1) 1
carbonic anhydrases - analysis (1) 1
carbonyl compounds (1) 1
catalysis, phase‐transfer catalysis (1) 1
cell line (1) 1
cell survival (1) 1
cells (1) 1
chemical reactions (1) 1
chemistry (1) 1
chemistry, medicinal (1) 1
click chemistry (1) 1
complexes (1) 1
concise total-synthesis (1) 1
coupling (1) 1
cross coupling (1) 1
cyanobacterium nostoc-muscorum (1) 1
cyclization (1) 1
cycloaddition (1) 1
cycloaddition reaction (1) 1
c‐c bond formation (1) 1
c−h arylation (1) 1
c−h coupling (1) 1
ch functionalization (1) 1
decarbonylative coupling (1) 1
decarboxylative arylation (1) 1
design (1) 1
direct arylation (1) 1
directed ortho borylation (1) 1
diversification (1) 1
electrophilic displacement reactions (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Chemical Communications, ISSN 1359-7345, 11/2017, Volume 53, Issue 88, pp. 11972 - 11983
Endogenous protein labeling is one of the most invaluable methods for studying the bona fide functions of proteins in live cells. However, multi-molecular... 
DEUBIQUITINATING ENZYME | SMALL-MOLECULE | IN-VIVO | TARGET IDENTIFICATION | DIRECTED TOSYL CHEMISTRY | PROTEASE ACTIVITY | CHEMISTRY, MULTIDISCIPLINARY | RHODIUM CARBENOIDS | CYSTEINE PROTEASES | ACTIVITY-BASED PROBES | LIVING CELLS
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 11/2017, Volume 53, Issue 88, pp. 11972 - 11983
Endogenous protein labeling is one of the most invaluable methods for studying the bona fide functions of proteins in live cells. However, multi-molecular... 
Cell Line | Molecular Probes - analysis | Molecular Probes - chemistry | Animals | Cell Survival | Humans | Staining and Labeling | Proteins - analysis | Kinetics | Proteins - chemistry
Journal Article
Tetrahedron, ISSN 0040-4020, 06/2017, Volume 73, Issue 26, pp. 3669 - 3676
We have achieved a synthesis of multiply arylated pyridines by using a [4 + 2] cycloaddition of 2,4-diaryl-5-chloroxazoles and cinnamic acids as a key... 
Ring transformation | Palladium | Pyridine | Cross-coupling | Heterocyclic compound | NICKEL CATALYSIS | ACIDS | STRATEGY | OXAZOLES | CHEMISTRY, ORGANIC | KETONES | ESTERS | DERIVATIVES | CYCLIZATION | ACCESS
Journal Article
ACS Medicinal Chemistry Letters, ISSN 1948-5875, 05/2014, Volume 5, Issue 5, pp. 582 - 586
We previously reported the discovery of NCH-31, a potent histone deacetylase (HDAC) inhibitor. By utilizing our C–H coupling reaction, we rapidly synthesized... 
Histone deacetylase | inhibitor | C-H coupling | HDAC6 | CELLS | DESIGN | CHEMISTRY, MEDICINAL | DIVERSIFICATION | ARYLATION | BOND FUNCTIONALIZATION | RECEPTOR | CANCER | ARYLBORONIC ACIDS | BORONIC ACIDS | HISTONE DEACETYLASE INHIBITORS
Journal Article
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, ISSN 0037-9980, 2013, Volume 71, Issue 6, pp. 576 - 587
Journal Article
ACS Central Science, ISSN 2374-7943, 09/2019, Volume 5, Issue 9, pp. 1541 - 1553
γ-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the central nervous system. The fast inhibitory actions of GABA are mainly mediated by... 
Journal Article
ACS Central Science, ISSN 2374-7943, 09/2019, Volume 5, Issue 9, pp. 1541 - 1553
Journal Article
09/2019
The present disclosure provides a labeling method for biological samples, the method comprising: (a) a step in which an immobilizing agent is applied to a... 
TESTING | INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES | MEASURING | PHYSICS
Patent
ChemInform, ISSN 0931-7597, 04/2015, Volume 46, Issue 15, p. no
The title reaction is used as the key step in the synthesis of lamellarins C and I (VII). 
Catalysis
Journal Article
01/2016, ISBN 9783527338887, 46
The synthesis of natural products and pharmaceuticals, particularly those containing heterocyclic frameworks, can be dramatically simplified by using catalytic... 
natural products | heteroaromatics | CH functionalization | pharmaceuticals | heterocycles | Heterocycles | C-H functionalization | Heteroaromatics | Natural products | Pharmaceuticals
Book Chapter
ChemInform, ISSN 0931-7597, 04/2015, Volume 46, Issue 15, pp. no - no
The title reaction is used as the key step in the synthesis of lamellarins C and I (VII). 
catalysis, phase‐transfer catalysis | pyrrole derivatives | regioselective reactions | alkaloids | C‐C bond formation
Journal Article
08/2014
Provided is an easy method (coupling method) capable of easily synthesizing a compound group in which aromatic molecules and aromatic molecules are coupled, a... 
METALLURGY | APPARATUS THEREFOR | ORGANIC CHEMISTRY | CHEMISTRY | HETEROCYCLIC COMPOUNDS | GENERAL METHODS OF ORGANIC CHEMISTRY
Patent
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.