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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 electronic resource (234 p.)
Soggetto topico Research & information: general
Soggetto non controllato cross coupling
dearomatization
C-H functionalization
indolin-3-ones
dimerization and trimerization of indoles
C-H borylation
Sonogashira cross-coupling
borylated aryl alkynes
one-pot reaction
restricted rotations
M(CO)3 tripods
molecular brakes and gears
X-ray
V-T NMR
borylation
Suzuki coupling
NH-Free
5-aryl pyrrole-2-carboxylates
iridium-catalyzed
heteroaryl substituted pyrroles
2,3'-bipyrrole
electrophilic haloacetylenes
pyrroles
ethynylpyrroles
furans
thiophenes
pyrazoles
Al2O3
transition-metal catalysis
intramolecular cyclization
medium-sized heterocycles
C-H activation
acylation
palladium
arenes
heteroarenes
indigo dyes
DSSC
synthesis
spectroscopy
Heck reaction
styrene
methoxycarbonylation
profene
cross-coupling reactions
C-C bond forming reactions
C-Heteroatom bond forming reactions
clinical candidate
DNA-encoded libraries
cyclopeptides
allosteric modulators
PROTAC
catalysis in water
C-C cross-coupling
Suzuki-Miyaura reaction
sulfonated salan
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
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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 electronic resource (160 p.)
Soggetto topico Research & information: general
Soggetto non controllato pillar[5]arene
planar chirality
chiral resolution
racemization kinetics
supramolecular chemistry
self-induced diastereomeric anisochronism (SIDA)
enantiomeric analysis
molecular association
NMR
diffusion
molecular chirality
self-disproportionation of enantiomers (SDE)
indole
asymmetric synthesis
organocatalysis
transition-metal catalysis
C-N bond formation
enantioselective
heterocycles
porphyrinoids
multinuclear complexes
chiral ligands
circular dichroism
paramagnetic NMR
magnetochemistry
porphyrin
guanidine
host-guest binding
chirality
DFT
TD-DFT simulation
induced optical activity
stereodynamic chirality probe
exciton coupling
circularly polarized luminescence
sergeants-and-soldiers
majority-rule
polysilane
polyfluorenevinylene
polyfluorene
mirror symmetry breaking
parity violation
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 electronic resource (172 p.)
Soggetto topico Research & information: general
Soggetto non controllato N-heterocyclic carbenes (NHC)
Lewis acid
cooperative catalysis
asymmetric synthesis
umpolung
amines
imines
photoredox catalysis
radical additions
radical-radical couplings
stereoselectivity
umpolung chemistry
visible light
proline
organocatalysis
asymmetric aldol reaction
methanol/water mixtures
sustainability
asymmetric catalysis
salen complexes
ring-opening
epoxide
kinetic resolution
organic electrosynthesis
electrochemistry
enantioselectivity
transition-metal catalysis
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