5 article(s) from Konno, Tsutomu
Graphical Abstract
Figure 1: Indenol skeleton.
Scheme 1: Synthesis of 2,3-disubstituted indene derivatives.
Scheme 2: Cobalt-catalyzed [2 + 3] cycloaddition reaction of the fluorinated alkynes 1 with various 2-formylp...
Scheme 3: Synthesis of the fluoroalkylated indenone 6 and the indanone 7 from the indenol 3aA. The yields wer...
Scheme 4: Stereochemical assignment of 5aA and 7 based on NMR techniques. The cross-peaks were observed throu...
Scheme 5: Proposed reaction mechanism.
Graphical Abstract
Figure 1: (A) Transition-metal-containing and (B) pure organic phosphorescent materials reported thus far (bp...
Figure 2: (A) Chemical structures of fluorescent bistolane derivatives previously developed by our group and ...
Scheme 1: Synthetic pathway for fluorinated benzil (2) and bisbenzil (3) derivatives.
Scheme 2: Proposed mechanism of Pd(II)-catalyzed alkyne oxidation by dimethyl sulfoxide (DMSO).
Figure 3: Mulliken charge distributions of fluorinated 1a and nonfluorinated 1c obtained from density functio...
Figure 4: Absorption and photoluminescence (PL) spectra of (A) 2a, (B) 2b, (C) 3a, (D) 3b, and (E) 3c in tolu...
Figure 5: Distributions of molecular orbitals (isosurface value: 0.04 a.u.) involved in vertical electronic t...
Graphical Abstract
Figure 1: Functional molecules with CF2CF2-fragment.
Scheme 1: Preparation and synthetic applications of 2-Zn.
Figure 2: Recovery yield of 2-Zn in DMF (ca. 0.70 M) after stirring at various temperature conditions.
Figure 3: Copper(I)-catalyzed cross-coupling reaction of 2-Zn with various iodoarene derivatives. NMR (isolat...
Scheme 2: Multigram-scale cross-coupling of 2-Zn with iodoarenes.
Scheme 3: Synthesis of a CF2CF2 group containing tolane derivative.
Figure 4: Copper(I)-catalyzed cross-coupling reaction of 2-Zn with various acid chlorides. NMR yields (isolat...
Graphical Abstract
Figure 1: Typical examples of previously reported negative-type liquid crystals containing a CF2CF2-carbocycl...
Scheme 1: Improved short-step synthetic protocol for multicyclic mesogens 1 and 2.
Scheme 2: Short-step approach to CF2CF2-containing carbocycles.
Figure 2: (a) Expected products of over-reaction in the Grignard reaction of dimethyl tetrafluorosuccinate (7...
Scheme 3: Mechanism for the reaction of γ-keto ester 6 with vinyl Grignard reagents.
Scheme 4: First multigram-scale preparation of CF2CF2-containing multicyclic mesogens.
Scheme 5: Stereochemical assignment of the ring-closing metathesis products.
Graphical Abstract
Figure 1: trans-Enediyne.
Scheme 1: Synthetic strategy for the preparation of trifluoromethylated diynes.
Scheme 2: Preparation of various enynes.
Figure 2: Regio- and stereoisomers.
Scheme 3: A proposed reaction mechanism.
Scheme 4: Synthesis of trans-enediynes. aDetermind by 19F NMR. Values in parentheses are of isolated yield.