Related references
Note: Only part of the references are listed.Synthesis and crystal structures of chiral ferrocene and ruthenocene substituted aminomethylnaphthols obtained through Betti-condensation
Krasimira Dikova et al.
POLYHEDRON (2019)
Recent advances in the synthesis and synthetic applications of Betti base (aminoalkylnaphthol) and bis-Betti base derivatives
Abolfazl Olyaei et al.
RSC ADVANCES (2019)
Phosgene invites selective switch-on fluorescence at ppm concentrations in a Betti base by hindering 2-way PET
Ankita Gangopadhyay et al.
NEW JOURNAL OF CHEMISTRY (2019)
Simple and Efficient Synthesis of Novel bis-Betti Bases via a One-Pot Pseudo-Five-Component Reaction
Abolfazl Olyaei et al.
LETTERS IN ORGANIC CHEMISTRY (2017)
Stereoselection in the Betti reaction of valine methyl esters
Maria Annunziata M. Capozzi et al.
TETRAHEDRON-ASYMMETRY (2017)
Bioactivity of a Family of Chiral Nonracemic Aminobenzylnaphthols towards Candida albicans
Maria Annunziata M. Capozzi et al.
MOLECULES (2014)
Synthesis and antimosquito properties of 2,6-substituted benzo[d]thiazole and 2,4-substituted benzo[d]thiazole analogues against Anopheles arabiensis
Katharigatta Narayanaswamy Venugopala et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2013)
Syntheses, transformations and applications of aminonaphthol derivatives prepared via modified Mannich reactions
Istvan Szatmari et al.
TETRAHEDRON (2013)
Synthesis of 1,3-aminonaphthols by diastereoselective Betti-type aminoalkylation of dihydroxy naphthalenes; diastereoselectivity, absolute configuration, and application
Maya Marinova et al.
TETRAHEDRON-ASYMMETRY (2013)
An Efficient Green MCR Protocol for the Synthesis of New Betti Bases via Mannich-Type Reaction
Abolfazl Olyaei et al.
LETTERS IN ORGANIC CHEMISTRY (2012)
An efficient, expeditious, and diastereoselective one-pot pseudo-five-component reaction for the synthesis of new bis-Betti bases under catalyst-free conditions
Mehdi Shafiee et al.
TETRAHEDRON LETTERS (2012)
Structural Influence of Chiral Tertiary Aminonaphthol Ligands on the Asymmetric Phenyl Transfer to Aromatic Aldehydes
Hui Wei et al.
CHIRALITY (2011)
Design, synthesis and bioevaluation of novel candidate selective estrogen receptor modulators
Yogesh Yadav et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2011)
A competent pot and atom-efficient synthesis of Betti bases over nanocrystalline MgO involving a modified Mannich type reaction
Bikash Karmakar et al.
TETRAHEDRON LETTERS (2011)
In vitro and in vivo multidrug resistance reversal activity by a Betti-base derivative of tylosin
N. Gyemant et al.
BRITISH JOURNAL OF CANCER (2010)
Simple and Efficient Procedure for the Synthesis of Novel 1,3-Diphenyl-2-azaphenalene Derivatives via One-Pot Multicomponent Reactions
Naser Foroughifar et al.
SYNTHETIC COMMUNICATIONS (2010)
Non-ionic surfactant catalyzed synthesis of Betti base in water
Atul Kumar et al.
TETRAHEDRON LETTERS (2010)
The Betti base: the awakening of a sleeping beauty
Cosimo Cardellicchio et al.
TETRAHEDRON-ASYMMETRY (2010)
Synthesis of Enantiopure 2-(Aminoalkyl)phenol Derivatives and Their Application as Catalysts in Stereoselective Reactions
Cristina Cimarelli et al.
CHIRALITY (2009)
Microwave-Assisted One-Pot Synthesis of (Aminoalkyl)naphthols and (Aminoalkyl)quinolinols by Using Ammonium Carbamate or Ammonium Hydrogen Carbonate as Solid Ammonia Source
Istvan Szatmari et al.
SYNTHESIS-STUTTGART (2009)
One-pot preparation of bis-Betti base product
Ren-Gen Xiong
LETTERS IN ORGANIC CHEMISTRY (2008)
Microwave-assisted, highly enantioselective addition of diethylzinc to aromatic aldehydes catalyzed by chiral aminonaphthols
Istvan Szatmari et al.
TETRAHEDRON-ASYMMETRY (2008)
Microwave-assisted synthesis of novel 2-naphthol bis-Mannich Bases
Po-Jung J. Huang et al.
ARKIVOC (2008)
A short history of SHELX
George M. Sheldrick
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES (2008)
Water promoted one-pot synthesis of 2'-aminobenzothiazolomethyl naphthols and 5-(2'-aminobenzothiazolomethyl)-6-hydroxyquinolines
Ahmad Shaabani et al.
TETRAHEDRON LETTERS (2007)
New macrocyclic compound as chiral shift reagent for carboxylic acids
Fengnian Ma et al.
ORGANIC LETTERS (2007)
Synthesis of chiral vicinal diamines by highly diastereoselective three-component phenolic Mannich reaction: Temperature-dependent stereodivergency
C Rondot et al.
ORGANIC LETTERS (2005)
Syntheses and transformations of 1-(α-aminobenzyl)-2-naphthol derivatives
I Szatmári et al.
CURRENT ORGANIC SYNTHESIS (2004)
Substituent effects in the ring-chain tautomerism of 1,3-diaryl-2,3-dihydro-1H-naphth[1,2-e] [1,3]oxazines
I Szatmári et al.
TETRAHEDRON (2003)
Neuroprotective effects of the novel D-3/D-2 receptor agonist and antiparkinson agent, S32504, in vitro against 1-methyl-4-phenylpyridinium (MPP+) and in vivo against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP): a comparison to ropinirole
JN Joyce et al.
EXPERIMENTAL NEUROLOGY (2003)
A practical stereoselective synthesis of secondary and tertiary aminonaphthols: chiral ligands for enantioselective catalysts in the addition of diethylzinc to benzaldehyde
C Cimarelli et al.
TETRAHEDRON-ASYMMETRY (2002)
The application of chiral aminonaphthols in the enantioselective addition of diethylzinc to aryl aldehydes
DX Liu et al.
ORGANIC LETTERS (2001)
Chiral aminoalcohols with a menthane skeleton as catalysts for the enantioselective addition of diethylzinc to benzaldehyde
S Panev et al.
TETRAHEDRON-ASYMMETRY (2001)
New bis-steroidal axially chiral diols as ligands for the asymmetric addition of diethylzinc to aldehydes
K Kostova et al.
TETRAHEDRON-ASYMMETRY (2000)
A practical o-hydroxybenzylamines promoted enantioselective addition of dialkylzincs to aldehydes with asymmetric amplification
G Palmieri
TETRAHEDRON-ASYMMETRY (2000)