Recent Publication (2002-present)
2017
1.
Kaise,
A.; Ohta, K.; Shirata, C.; Endo, Y.
Design and Synthesis
of p-Carborane-containing Sulfamates
as Multitarget Anti-breast Cancer Agents
Bioorg. Med. Chem., 2017, 25, 6417-6426
2.
Kaise,
A.; Ohta, K.; Endo, Y.
Novel p-carborane-containing multitarget
anticancer agents inspired by the metabolism of 17b-estradiol
Bioorg. Med. Chem., 2017, 25, 6371-6378
3.
Ohta,
K.; Ogawa, T.; Endo, Y.
Design and
synthesis of iodocarborane-containing ligands with high affinity and
selectivity toward ERb
Bioorg. Med. Chem. Lett., 2017, 27, 4030?4033
4.
Taguchi,
R.; Hatayama, K.; Takahashi, T.; Hayashi, T.; Sato, Y.; Sato, D.; Ohta, K.; Nakano,
H.; Seki, C.; Endo, Y.; Tokuraku, K.; Uwai, K.
Structureactivity
relations of rosmarinic acid derivatives for the amyloid b aggregation inhibition and antioxidant
properties
Eur.
J. Med. Chem., 2017, 138,
1066-1075
2016
5.
Watanabe,
K.; Hirata, M.; Tominari, T.; Matsumoto, C.: Endo, Y.; Murphy, G.; Nagase, H.; Inada,
M.; Miyaura, C.
BA321, a novel
carborane analog that binds to androgen and estrogen receptors, acts as a new
selective androgen receptor modulator of bone in male mice
Biochem. Biophys. Res. Commun., 2016, 478, 279?285
6.
Kaise,
A.; Ohta, K.; Endo, Y.
Design,
synthesis, and anti-proliferative activity of
1-(4-methoxyphenyl)-12-hydroxymethyl- p-carborane
derivatives
Eur. J. Med. Chem., 2016, 122, 257?263
7.
Sato,
M.; Ohta, K.; Kaise, A.; Aoto, S.; Endo, Y.
Symmetric
4,4'-(piperidin-4-ylidenemethylene)bisphenol derivatives as novel tunable
estrogen receptor (ER) modulators
Bioorg. Med. Chem. 2016, 24, 1089-1094
8.
Nakagawasai,
O.; Nemoto, W.; Onogi,@H.; Moriya, T.; Lin, J-R.
Odaira, T.; Yaoita, F.; Ogawa, T.; Ohta, K.; Endo, Y.; Tan-No, K.
BE360, a new
selective estrogen receptor modulator, produces antidepressant and antidementia
effects through the enhancement of hippocampal cell proliferation in olfactory
bulbectomized mice
Behavioural Brain Research, 2016, 297, 315?322
2015
9.
Certo,
M.; Endo, Y.; Ohta, K.; Sakurada, S.; Bagetta, G.; Amantea, D.
Activation of
RXR/PPARg underlies neuroprotection by
bexarotene in ischemic stroke
Pharmacological
Research, 2015, 102, 298-307
10.
Kojima,
K.; Ogawa, T.; Kitao, S.; Sato, M.; Oda, A.; Ohta, K.; Endo, Y.
Estrogenic
activity of bis(4-hydroxyphenyl)methanes with cyclic hydrophobic structure
Bioorg. Med. Chem., 2015, 23, 6900-6911
11.
Ohta,
K.; Ogawa, T.; Oda, A.; Kaise, A.; Endo, Y.
Design and
synthesis of carborane-containing estrogen receptor-beta (ERb)-selective ligands
Bioorg. Med. Chem. Lett, 2015, 25, 4174?4178
12.
Ohta,
K.; Ogawa, T.; Kaise, A.; Endo, Y.
Synthesis and
biological evaluation of novel m-carborane-containing estrogen receptor partial
agonists as SERM candidates
Bioorg. Med. Chem. Lett, 2015, 25, 3213?3216
13.
Ohta,
K.; Chiba, Y.; Kaise, A.; Endo, Y.
Structure?activity
relationship study of diphenylamine-based estrogen receptor (ER) antagonists
Bioorg. Med. Chem., 2015, 23, 861?867
2014
14.
Inomata,
K.; Endo, Y.
Synthesis of
2-substituted 1,3-cycloheptanedione via a Lewis acid mediated ring expansion
reaction
Heterocycles, 2014,
88, 997-1012
15.
Muroi,
Y.; Saito, T.; Takahashi, M.; Sakuyama, K.; Niinuma, Y.; Ito, M.; Tsukada, C.; Ohta,
K.; Endo, Y.; Oda, A.; Hirasawa, N.; Hiratsuka, M.
Functional characterization
of wild-type and 49 CYP2D6 allelic variants for N-desmethyltamoxifen
4-hydroxylation activity
Drug Metab. Pharmacok. 2014, 29, 360-366
16.
Ohta,
K.; Ogawa, T.; Kaise, A.; Endo, Y.
Novel Estrogen
Receptor (ER) Modulators Containing Various Hydrophobic Bent- Core Structures
Bioorg. Med. Chem. 2014, 22, 3508-3514
17.
Ohta,
K.; Ogawa, T.; Kaise, A.; Oda, A.; Endo, Y.
Aliphatic
Substitution of o-Carboranyl Phenols Enhances Estrogen Receptor Beta
Selectivity
Chem. Pharm. Bull., 2014, 62, 386-391
2013
18.
Ohta,
K.; Ogawa, T.; Kaise, A.; Endo, Y.
Enhanced
Estrogen Receptor beta (ERb) Selectivity of Fluorinated Carborane-containing
ER Modulators
Bioorg. Med. Chem. Lett., 2013, 23, 6555-6558
19.
Inomata,
K.; Endo, Y.
Synthesis of
2-?Substituted 1,?3-?Cycloheptanedionevia a Lewis Acid Mediated Ring Expansion Reaction
Heterocycles, 2013, 88, 997-1012
20.
Ohta,
K.; Ogawa, T.; Kaise, A.; Oda, A.; Endo, Y.
Aliphatic
Substitution of o-Carboranyl Phenols Enhances Estrogen Receptor Beta
Selectivity
Chem. Pharm. Bull., 2013, 62, 386-391
21.
Ohta,
K.; Kawachi, E.; Shudo, K.; Kagechika, H.
Structure-activity
Relationship Study on Benzoic Acid Part of Diphenylamine-based Retinoids
Bioorg.
Med. Chem. Lett., 2013, 23, 81-84
2012
22.
Ohta,
K.; Ogawa, T.; Endo, Y.
Estrogenic
Activity of B-Fluorinated o-Carborane-1,2-bisphenol
Synthesized via SNAr Reaction
Bioorg. Med. Chem., 2012, 20, 4728-4730
23.
Fujii,
S.; Ohta, K.; Goto, T.; Oda, A.; Masuno, H.; Endo, Y.; Kagechika, H.
Development of
Androgen Receptor Ligands by Application of Ten-vertex p-Carborane as a Novel
Hydrophobic Core Structure
Med. Chem. Commun., 2012, 3, 680-684
24.
Ohta, K.; Taguchi, F.; Endo, Y.
Facile
Synthesis and Estrogenic Activity of Arylpyrrole-based Bisphenol Derivatives
Heterocycles, 2012, 86, 165-170
2011
25.
Fujii, S.; Masuno, H.; Taoda, Y.; Kano, A.; Wongmayura, A.;
Nakabayashi, M.; Ito, N.; Shimizu, M.; Kawachi, E.; Hirano, T.; Endo, Y.;
Tanatani, A.; Kagechika, H.
Boron
Cluster-based Development of Potent Non-Secosteroidal Vitamin D Receptor
Ligands: Direct Observation of Hydrophobic Interaction between Protein Surface
and Carborane
J. Am. Chem. Soc. 2011,
133, 20933-20941
26.
Ohta,
K.; Goto, T.; Fujii, S.; Kawahata, M.; Oda, A.; Ohta, S.; Yamaguchi, K.; Hirono,
S.; Endo, Y.*
Crystal Structure,
Docking Study and Structure?activity Relationship of Carborane-containing Androgen
Receptor Antagonist 3-(12-Hydroxymethyl-1,12-dicarba-closo-dodecaboran-1-yl)-
benzonitrile.
Bioorg. Med. Chem., 2011,
19, 3540-3548
27. Ohta, K.; Kawachi,
E.; Fukasawa, H.; Shudo, K.; Kagechika, H.
Diphenylamine-based
Retinoid Anatagonists: Regulation of RAR and RXR Function Depending on the
N-substituent
Bioorg.
Med. Chem., 2011, 19, 2501-2507
28.
Fujii,
S.; Yamada, A.; Tomita, K.; Nagano, M.; Goto, T.; Ohta, K.; Harayama, T.; Endo,
Y.; Kagechika, H.
p-Carborane Based Androgen Antagonists
Active in LNCaP Cells with a Mutated Androgen Receptor
Med. Chem. Commun., 2011, 2, 877-880
29.
Wietrzych-Schindler,
M.; Szyszka-Niagolov, M.; Ohta, K.; Endo, Y.; Perez, E.; de Lera, A. R.;
Chambon, P.; Krezel, W.
Retinoid X
Receptor Gamma Is Implicated in Docosahexaenoic Acid Modulation of Despair
Behaviors and Working Memory in Mice.
Biol.
Psychiatry, 2011, 69, 788-794.
30.
Akahane,
Y.; Inomata, K.; Endo, Y.
Asymmetric Intramolecular
Aldol Reaction Mediated by (S)-N-Substituted -N-(2-pyrrolidinylmethyl)amine
to Prepare Wieland-Miescher Ketone.
Heterocycles, 2011, 82: 1727-1737.
2010
31.
Songkram,
C.; Ohta, K.; Yamaguchi, K.; Pichierri, F.; Endo, Y.*
Conformational
Control of Benzyl-o-carboranylbenzene Derivatives and Molecular
Encapsulation of Acetone into the Dynamically-formed Space of
1,3,5-Tris(2-benzyl-o- carboran-1-yl)benzene.
Inorg. Chem., 2010, 49, 11174?11183.
32.
Goto,
T.; Ohta, K., Fujii, S.; Ohta, S.; Endo, Y.*
Design and
Synthesis of Androgen Receptor Full Antagonists Bearing a p-Carborane Cage:
Promising Ligands for Anti-androgen Withdrawal Syndrome.
J. Med.
Chem., 2010,
53, 4917?4926.
33.
Aizawa,
K.; Ohta, K., Endo, Y.*
Synthesis of
3-Aryl-1,2-dicarba-closo-dodecaboranes by Suzuki-Miyaura Coupling
Reaction.
Heterocycles,
2010, 80: 369-377.
2009
34.
Jankowiak,
A.; Kaszynski, P.*; Tilford, W. R.; Ohta, K.; Januszko, A.; Nagamine, T.; Endo,
Y.
Ring-alkyl
Connecting Group Effect on Mesogenic Properties of p-Carborane
Derivatives and Their Hydrocarbon Analogues.
Beil, J. Org.
Chem., 2009,
5, 1-9.
35.
Ohta,
K.; Ogawa, T.; Suzuki, T.; Ohta, S.; Endo. Y.*
Novel Estrogen
Receptor (ER) Modulators: Carbamate and Thiocarbamate Derivatives with m-Carborane
Bisphenol Structure.
Bioorg. Med. Chem., 2009,
17, 7958-7963.
36.
Ohta, K.; Yamazaki, H.; Endo, Y.*
Magnesium-Assisted
Intramolecular Demethylation Utilizing Carborane C-H Geometry
37.
Ohta, K.; Konno, S; Endo, Y.*
Complexation of a-Cyclodextrin with Carborane
Derivatives in Aqueous Solution
Chem.Pharm. Bull., 2009, 57, 3-7-310.
38.
Ogawa,
T.; Ohta, K.; Iijima, T.; Suzuki, T.; Ohta, S.; Endo, Y.*
Synthesis and Biological
Evaluation of p-Carborane Bisphenols and Their Derivatives: Structure-activity
Relationship for Estrogenic Activity
Bioorg. Med. Chem., 2009, 17,
1109-1117.
39.
Akahane,
Y.; Inomata, K.; Endo, Y.
A new chiral synthesis of
Wieland-Miescher ketone catalyzed by a combination of (S)-N-benzyl-(2-pyrrolidinylmethyl)amine
derivative and Bronsted acid.
Heterocycles, 2009, 77,
1065-1078.
40.
Hirata,
M.; Inada, M.; Matsumoto, C.; Takita, M.; Ogawa, T.; Endo, Y.; Miyaura, C.*
A novel carborane Analog,
BE360, with a Carbon-containing polyhedral Boron-cluster Is a New Selective
Estrogen Receptor Modulator for Bone.
Biochem. Biophys. Res. Commun., 2009,
380, 218-222.
2008
41.
Kaszynski,
P.*; Januszko, A.; Ohta, K.; Nagamine, T.; Potaczek, P.; Young, V. G. Jr.; Endo,
Y. Conformational effects on mesophase stability: Numerical comparison of carborane
diester homologous series with thier bicyclo[2,2,2]octane, cyclohexane and
benzene analogues
Liq. Cryst., 2008, 35, 1169-1190.
42.
Fujii,
S.; Ohta, K.; Goto, T.; Kagechika, H.; Endo, Y.*
Acidic Heterocycles As Novel Hydrophilic
Pharmacophore of Androgen Receptor Ligands with a Carborane Core Structure
Bioorg. Med. Chem., 2009, 17,
344-350.
43.
Ohta, K.; Konno, S; Endo, Y.*
Complexation of b-Cyclodextrin with Carborane
Derivatives in Aqueous Solution
Tetrahedron
Lett.
2008, 49, 6525-6528.
44.
Ohta, K.; Chiba, Y.; Ogawa, T.; Endo,
Y.*
Promising Core Structure for
Nuclear Receptor Ligands: Design and Synthesis of Novel Estrogen Receptor
Ligands Based on Diphenylamine Skeleton
Bioorg. Med. Chem. Lett., 2008,
18, 5050-5053.
45.
Goto,
T.; Fijii, S.; Suzuki, T.; Ohta, S.; Endo, Y.*
Design and Synthesis of Carborane-containing
Androgen Receptor (AR) Antagonist Bearing a Pyridine Ring
Bioorg. Med. Chem., 2008, 16, 8022-8028.
46.
Nagamine,
T.; Inomata, K.*; Endo, Y.
A New Chiral Synthesis of a
Bicyclic Endione Containing a Seven-membered Ring Mediated by a Combination of
Chiral Amine and Bronsted Acid
Heterocycles, 2008, 76, 1191-1204.
47.
Nagamine,
T.; Januszko, A.; Ohta, K.; Kaszynski, P.; Endo. Y.
The
effect of the linking group on mesogenic properties of three-ring derivatives of
p-carborane and biphenyl
Liq. Cryst. 2008, 35, 865?884.
48.
Pociecha
, D.; Ohta, K.; Januszko, A.; Kaszynski, P.*; Endo, Y.
Symmetric Bent-core Mesogens
with m-Carborane and Adamantane As the Central Units
J. Mater. Chem., 2008, 18, 2978 - 2982.
49.
Taoda,
Y.; Sawabe, T.; Endo, Y.*; Yamaguchi, K.; Fujii, S.; Kagechika, H.*
Identification of an Intermediate in the Deboronation of ortho-Carborane: an Adduct of ortho-Carborane with Two Mucleophiles on One Boron Atom
Chem. Commun., 2008, 2049-2051.
50. Akahane, Y.; Inage, N.; Nagamine, T.; Inomata, K.*; Endo, Y.
An Alternative Chiral Synthesis of Wieland-Miescher Ketone Mediated by (S)-2-(Pyrrolidinylmethyl)pyrrolidine: Remarkable Effects of Bronsted Acid
Heterocycles, 2008, 74, 637-648.
2007
51. Ohta, K.; Yamazaki, H.; Pichierri , F.; Kawahata, M.; Yamaguchi, K.; Endo, Y.*
Solid-state Supramolecular Array through Cooperative p-p Interactions of 1-(2-Methoxyphenyl)-o-carborane
Tetrahedron, 2007, 63, 12160-12165.
52. Nagamine, T.; Inomata, K.*; Endo, Y.*
Enantioselective Intramolecular Aldol Reaction Mediated by a Combination of L-Amino Acid and Bronsted Acid to Construct a New Bicyclic Enedione Containing a 7-Membered Ring
Chem.Pharm. Bull., 2007, 55, 1710-1712.
53. K. Ohta, K.; Yamazaki, H.; Kawahata, M.; Yamaguchi, K.; Pichierri, F.; Endo, Y.*
Proton-Driven Conformational Change in a 2-Aryl-p-carborane Constrained by an Intramolecular C-H---O Hydrogen Bond
Tetrahedron. Lett., 2007, 48, 5231-5234.
54. Ohta, K.; Goto, T.; Yamazaki, H.; Pichierri, F.: Endo, Y.*
Facile and Efficient Synthesis of C-Hydroxycarboranes and C,C'-Dihydroxycarboranes
Inorg. Chem., 2007, 46, 3966-3970
55. Nagamine, T.; Inomata, K.*; Endo, Y.; Paquette, L. A.
Amino Acid-mediated Intramolecular Asymmetric Aldol Reaction to Construct a New Chiral Bicyclic Enedione Containing a 7-Membered Ring: Remarkable Inversion of Enantioselectivity Compared to the 6-Membered Ring.
J. Org. Chem., 2007, 72, 123-131.
2006
56. Nagamine, T.; Januszko, A.; Kaszynski, P.*; Ohta, K.; Endo, Y.
J. Mater. Chem., 2006, 6, 3836-3843.
57. Calleja, C.; Messaddeq, N.; Chapellier, B.; Yang, H.; Krezel, W.; Li, M.; Metzger, D.; Marcrez, B.; Ohta, K.; kagechika, H,; Endo, Y.; Mark, M.; Ghyselinck, N. B.; Chambon, P.*
Genetic and Pharmacological Evidence that a Retinoic Acid Cannot be the RXR-activating Ligand in Mouse Epidermis Keratinocytes.
Genes Dev., 2006, 20, 1525 - 1538.
58. Ogawa, T.; Ohta, K.; Yoshimi, T.; Yamazaki, H.; Suzuki, T.; Ohta, S.; Endo, Y.*
m-Carborane Bisphenol Structure as a Pharmacophore for Selective Estrogen Receptor Modulators
Bioorg. Med. Chem. Lett., 2006, 16, 3943-3946.
59. Ohta, K.; Yamazaki, H.; Endo, Y.*
NMR Study of 1,2-Dicarba-closo-dodecaboranes: Intramolecular C-H---O Hydrogen Bonding in Solution.
Tetrahedron. Lett., 2006, 47, 1937-1940.
2005
60. Ohta, K.; Goto, T.; Endo, Y.*
1,2-Dicarba-closo-dodecaboran-1-yl Naphthalene Derivatives.
Inorg. Chem., 2005, 23, 8569-8573.
61. Nagamine, T.; Januszko, A.; Ohta, K.; Kaszynski, P.; Endo, Y.
A comparison of Mesogenic Properties of p-Carborane-1,12-dicarbaldehyde Schiff Bases with Their Terephthaldehyde Analogues.
Liq. Cryst. 2005, 32, 985-995.
62. Goto, T.; Ohta, K.; Suzuki, T.; Ohta, S.; Endo, Y.*
Bioorg. Med. Chem., 2005, 13, 6414-6424.
63. Fujii, S.; Goto, T.; Ohta, K.; Hashimoto, Y.; Suzuki, T.; Ohta, S.; Endo, Y.*
Potent Androgen Antagonists Based on Carborane As a Hydrophobic Core Structure.
J. Med. Chem. 2005, 48, 4654-4662.
64. Endo, Y*.; Yoshimi, T.; Ohta, K.; Suzuki, T.; Ohta, S.
Potent Estrogen Receptor Ligands Based on Bisphenols with Globular Hydrophobic Cores.
J. Med. Chem. 2005, 48, 3941-3944.
65. Endo, Y.*; Songkram, C.; Ohta, K.; Yamaguchi, K.
Synthesis of Distorted Molecules Based on Spatial Control with Icosahedral Carboranes
J. Organomet. Chem., 2005, 690, 2750-2756.
66. Yamazaki, H.; Ohta, K.; Endo, Y.*
Regioselective Synthesis of Triiodo-o-carboranes and Tetraiodo-o-carborane.
Tetrahedron
Lett., 2005, 46, 3119-3122.
67. Endo, Y.*; Songkram, C.; Ohta, K.; Kaszynski, P.; Yamaguchi, K.
A Distorted Benzene Bearing Two Bulky Substituents on Adjacent Positions: Structure of 1,2-Bis(1,2-Dicarba-closo-dodecaboran-1-yl)benzene.
Tetrahedron Lett., 2005, 46, 699-702.
68. Ohta, K.; Goto, T.; Endo, Y.*
New Synthetic Method of 1,2-Diaryl-1,2-dicarba-closo-dodecaboranes Employing Aromatic Nucleophilic Substitution (SNAr) Reaction.
Tetrahedron Lett., 2005, 46, 483-485.
69. Fujii, S.; Hashimoto, Y.; Suzuki, T.; Ohta, S.; Endo, Y*
A new Class of Androgen Receptor Antagonists Bearing Carborane in Place of a Steroidal Skeleton.
BioMed. Chem. Lett. 2005, 15, 227-230.
2004
70. Ohta, K.; Iijima, T.; Kawachi, E.; Kagechika, H.; Endo, Y*
Novel Retinoid X Receptor (RXR) Antagonists Having a Dicarba-closo-dodecaborane as a Hydrophobic Moiety.
BioMed. Chem. Lett. 2004, 14, 5913-5918.
71. Endo, Y.*; Ohta, K.; Yoshimi, T.; Yamaguchi, K. A New Application of Inorganic Cluster, Carboranes for Medicinal Drug Design and Molecular Construction.
Phosphorous, Sulfur, and Silicon. 2004, 179, 799-802.
72. Ohta, K.; Januszko, A.; Kaszynski, P.; Nagamine, T.; Sasnouski, G.; Endo, Y.
Structural Effects in Three-Ring Mesogenic Derivatives of p-Carborane and Their Hydrocarbon Analogs.
Liq. Cryst. 2004, 31, 1-12.
73. Suzuki, K.; Inomata, K.; Endo, Y.
Enantiocontrllooed Synthesis of Jasmonates via Tandem Retro-Diels-Alder-Ene reaction Activated by a Silyl Substituent
Org. Lett., 2004, 6, 409-411.
74. Taoda, Y.; Endo, Y.*
Electronic Effects of Icosahedral Carboranes: Mechanistic Alteration in Solvolysis of a-(o-Carboranyl)benzyl Tosylates by Electronic Effect of Substituents
Tetrahedron Lett., 2003, 44, 8177-8181.
75. Endo, Y.*; Yamamoto, K.; Kagechika, H.
Utility of Boron Clusters for Drug Design. Relation between Estrogen Receptor Binding Affinity and Hydrophobicity of Phenols Bearing Various Types of Carboranyl Groups.
BioMed. Chem. Lett. 2003, 13, 4089-4092.
76. Johnsamuel, J.; Byun, Y.; Jones, T. P.; Endo, Y.; Tjarks, W.
A Convenient Method for the Computer-Aided Molecular Design of Carborane Containing Compounds.
BioMed. Chem. Lett. 2003, 13,3213-3216.
77. Endo, Y.*; Yoshimi, T.; Miyaura, C.
Boron Clusters for Medicinal Drug Design: Selective Estrogen Receptor Modulators Bearing Carborane
Pure Appl. Chem., 2003, 75, 1197-1205.
78. Johnsamuel, J.; Byun, Y.; Jones, T. P.; Endo, Y.; Tjarks, W.
A New Strategy for Molecular Modeling and Receptor-based Design of Carborane Containing Compounds.
J. Organomet. Chem., 2003,
680, 223-231.
79. Suzuki, K.; Inomata, K.; Endo, Y.
New Chiral Synthesis Methyl and Allyl Disubstituted Butyro Lactone: A Formal Synthesis of (-)-Ngaione
Heterocycles, 2003, 60, 2743-2748.
2002
80.
Igarashi, Y.; Sekine, A.; Uehara, Y.;
Yamaguchi, K.; Endo,
Y.; Furumai, T.; Oki, T.
Anicequol, a
Novel Inhibitor for Anchorage-independent Growth of Tumor Cells from Penicillium sp. TP-F0213
J.
Antibiotics.,
2002, 55, 371-376.
81. Toya, T.; Fukasawa, H.; Masui, A.; Endo, Y.*
Potent and Selective Partial Ecdysone Agonist Activity of Chromafenozide in Sf9 Cells
Biochem. Biophys. Res. Commun., 2002, 292, 1087-1091.
82. Endo,Y.*; Songkram, C.; Yamasaki, R.; Tanatani, A.;Kagechika, H.;Takaishi, K.;Yamaguchi, K.
Molecular
Construction Based on Icosahedral Carboranes and Aromatic N,Nf-Dimethylurea Groups. Aromatic Layered Molecules and a
Transition Metal Complex
J. Organomet. Chem., 2002, 657, 48-58.
83. Toya, T.; Yamaguchi, K.; Endo, Y.*
Cyclic Dibenzoylhydrazines Reproducing the Conformation of Ecdyson Agonists, RH-5849. Importance of Hydrogen-bonding Character of NH Group
BioMed. Chem., 2002, 10, 953-961.