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Advances in Cross-Coupling Reactions
Advances in Cross-Coupling Reactions
Autore Pérez Sestelo José
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (234 p.)
Soggetto topico Research and information: general
Soggetto non controllato 2,3'-bipyrrole
5-aryl pyrrole-2-carboxylates
acylation
Al2O3
allosteric modulators
arenes
borylated aryl alkynes
borylation
C-C bond forming reactions
C-C cross-coupling
C-H activation
C-H borylation
C-H functionalization
C-Heteroatom bond forming reactions
catalysis in water
clinical candidate
cross coupling
cross-coupling reactions
cyclopeptides
dearomatization
dimerization and trimerization of indoles
DNA-encoded libraries
DSSC
electrophilic haloacetylenes
ethynylpyrroles
furans
Heck reaction
heteroarenes
heteroaryl substituted pyrroles
indigo dyes
indolin-3-ones
intramolecular cyclization
iridium-catalyzed
M(CO)3 tripods
medium-sized heterocycles
methoxycarbonylation
molecular brakes and gears
n/a
NH-Free
one-pot reaction
palladium
profene
PROTAC
pyrazoles
pyrroles
restricted rotations
Sonogashira cross-coupling
spectroscopy
styrene
sulfonated salan
Suzuki coupling
Suzuki-Miyaura reaction
synthesis
thiophenes
transition-metal catalysis
V-T NMR
X-ray
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557316703321
Pérez Sestelo José  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral Auxiliaries and Chirogenesis II
Chiral Auxiliaries and Chirogenesis II
Autore Borovkov Victor
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (160 p.)
Soggetto topico Research and information: general
Soggetto non controllato asymmetric synthesis
C-N bond formation
chiral ligands
chiral resolution
chirality
circular dichroism
circularly polarized luminescence
DFT
diffusion
enantiomeric analysis
enantioselective
exciton coupling
guanidine
heterocycles
host-guest binding
indole
induced optical activity
magnetochemistry
majority-rule
mirror symmetry breaking
molecular association
molecular chirality
multinuclear complexes
n/a
NMR
organocatalysis
paramagnetic NMR
parity violation
pillar[5]arene
planar chirality
polyfluorene
polyfluorenevinylene
polysilane
porphyrin
porphyrinoids
racemization kinetics
self-disproportionation of enantiomers (SDE)
self-induced diastereomeric anisochronism (SIDA)
sergeants-and-soldiers
stereodynamic chirality probe
supramolecular chemistry
TD-DFT simulation
transition-metal catalysis
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557757103321
Borovkov Victor  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
New Trends in Asymmetric Catalysis
New Trends in Asymmetric Catalysis
Autore Della Sala Giorgio
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Descrizione fisica 1 online resource (172 p.)
Soggetto topico Research and information: general
Soggetto non controllato amines
asymmetric aldol reaction
asymmetric catalysis
asymmetric synthesis
cooperative catalysis
electrochemistry
enantioselectivity
epoxide
imines
kinetic resolution
Lewis acid
methanol/water mixtures
N-heterocyclic carbenes (NHC)
n/a
organic electrosynthesis
organocatalysis
photoredox catalysis
proline
radical additions
radical-radical couplings
ring-opening
salen complexes
stereoselectivity
sustainability
transition-metal catalysis
umpolung
umpolung chemistry
visible light
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557355803321
Della Sala Giorgio  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2021
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui