Special Issue

Kenji Koga's Special Issues, Vol. 66, No. 1, 2005

84 data found. 61 - 84 listedFirst Previous
Note | Special issue | Vol 66, No. 1, 2005, pp.535-542
Published online: 22nd July, 2005
DOI: 10.3987/COM-05-S(K)5
Wittig Rearrangement of Ally 2-Thiophenemethyl Ethers: Facile Synthesis of Thiophenemethanol and -ethanol Derivatives

Masayoshi Tsubuki,* Sohichiro Matsuo, and Toshio Honda*

*Institute of Medical Chemistry, Hoshi University, 2-4-41 Ebara, Shinagawa-ku, Tokyo 142-8501, Japan

Abstract

Wittig rearrangement of allyl 2-thiophenemethyl ethers was studied. Deprotonation of allyl 2-thiophenemethyl ethers (1a-d) occurred preferentially either the α- or the α’-position, depending on three kinds of BuLi. Thiophenemethanol and -ethanol derivatives were obtained as products of [2,3] and [1,2] sigmatropic rearrangements, respectively.

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Note | Special issue | Vol 66, No. 1, 2005, pp.543-548
Published online: 2nd December, 2005
DOI: 10.3987/COM-05-S(K)6
Direct C-C Coupling of meso-Octamethylcalix[4]pyrrole with 6-Nitroazolopyrimidines

Oleg N. Chupakhin,* Nadezhda A. Itsikson, Sergey Sh. Bashirov, Dmitry G. Beresnev, and Gennady L. Rusinov

*Institute of Organic Synthesis, Urals Branch, Russian Academy of Sciences, 20, S. Kovalevskaya st., Ekaterinburg, GSP-147, 620219, Russia

Abstract

It has been found that the reaction of meso-octamethylcalix[4]pyrrole with four equivalents of 6-nitroazolopyrimidine is accompanied by the C-C coupling of unsubstituted carbon atom in azines with β-position of pyrrole rings and results in the formation of tetrapyrimidine-substituted calix[4]pyrroles without introduction of any catalysts. Mono- and di-substituted calixpyrroles have been isolated.

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Note | Special issue | Vol 66, No. 1, 2005, pp.549-555
Published online: 16th August, 2005
DOI: 10.3987/COM-05-S(K)7
Synthesis of (-)-5-Epiindolizidine 167B and Formal Synthesis of 5E,9Z-Indolizidine 223AB

Naoki Toyooka* and Hideo Nemoto

*Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama, Toyama 930-0194, Japan

Abstract

Synthesis of (-)-5-epiindolizidine 167B has been described using the highly stereoselective reduction of the enyne (2) as the key step.

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Note | Special issue | Vol 66, No. 1, 2005, pp.557-562
Published online: 20th September, 2005
DOI: 10.3987/COM-05-S(T)51
Heterocycles from Ylides. Part IX. A Convenient Synthesis of 1-Sulfonyl-2,3-disubstituted 2,3-Dihydroindoles

Giuseppe Cremonesi, Piero Dalla Croce,* and Concetta La Rosa

*Dipartimento di Chimica Organica e Industriale, Centro C. N. R., Università degli Studi di Milano, V. Venezian 21, I-20133 Milano, Italy

Abstract

The reaction of sulfur ylides (1) with N-(2-bromomethylphenyl)benzenesulfonamides (4) gives 2,3-dihydroindoles (5) whose structure and stereochemistry were assigned on the basis of analytical and spectroscopic data. Some chemical transformations of 5 are reported.

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Note | Special issue | Vol 66, No. 1, 2005, pp.563-566
Published online: 11th October, 2005
DOI: 10.3987/COM-05-S(K)19
Intermolecular Photoreaction of Benzenecarbothioamide with γ,δ-Unsaturated Ketones: Application to Synthesis of Cycloalkane [c]-Fused Pyridines

Kazuaki Oda,* Michiko Haneda, Naozumi Nishizono,* and Minoru Machida

*Faculty of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Hokkaido 061-0293, Japan

Abstract

Irradiation of benzenecarbothioamide with (2-methylenecycloalkyl)acetaldehyde in benzene gives cycloalkane [c]-fused pyridines in moderate yields.

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Note | Special issue | Vol 66, No. 1, 2005, pp.567-578
Published online: 18th October, 2005
DOI: 10.3987/COM-05-S(K)25
Dirhodium(II) Tetrakis[N-benzene-fused Phthaloyl-(S)-piperidinonate] as a Chiral Lewis Acid: Catalytic Enantioselective Aldol Reactions of Acetate-derived Silylketene Acetals and Aldehydes

Takuya Washio, Seiichi Nakamura, Masahiro Anada, and Shunichi Hashimoto*

*Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita 12 Nishi 6, Kita-ku, Sapporo, Hokkaido 060-0812, Japan

Abstract

A first example of chiral dirhodium(II) complex-catalyzed enantioselective Mukaiyama aldol reactions is described. The aldol addition reaction of methyl acetate-derived trimethylsilylketene acetal with specific aldehydes such as benzyloxyacetaldehyde and electron-poor aromatic aldehydes is effectively catalyzed by dirhodium(II) tetrakis[N-benzene-fused phthaloyl-(S)- piperidinonate] (1a), providing silylated aldol adducts in up to 94% ee.

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Note | Special issue | Vol 66, No. 1, 2005, pp.579-582
Published online: 4th October, 2005
DOI: 10.3987/COM-05-S(K)31
Synthesis of 3-O-Alkylascorbic Acids from L-Ascorbic Acid in a Single Step

Yasuo Kikugawa,* Takeshi Sakamoto, Shinya Sato, and Kayoko Asami

*Faculty of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295, Japan

Abstract

An efficient single step synthesis of 3-O-alkylascorbic acids from ascorbic acid is described.

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Note | Special issue | Vol 66, No. 1, 2005, pp.583-594
Published online: 18th October, 2005
DOI: 10.3987/COM-05-S(K)33
Solvent Effect on the Reaction of 1-Methoxy-3-(2-nitrovinyl)indole with Nucleophiles

Koji Yamada, Tomoyuki Izumi, Fumio Yamada, and Masanori Somei*

*Division of Pharmaceutical Sciences, Graduate School of Natural Science and Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa 920-1192, Japan

Abstract

1-Methoxy-3-(2-nitrovinyl)indole (1a) functions as an electrophile and reacts with various nucleophiles. In THF, nucleophiles undergo conjugate addition to the β-carbon of the nitrovinyl side chain of 1a, regioselectively. The resultant Michael addition products (4d and 8) cyclize to novel 3-substituted 1-methoxyindoles (5 and 7) depending on reaction conditions and a plausible mechanism is discussed. In dipolar aprotic solvent (DMF), nucleophiles react with 1a at the 2-position predominantly with concomitant liberation of the 1-methoxy group giving 2-substituted indoles.

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Note | Special issue | Vol 66, No. 1, 2005, pp.595-602
Published online: 1st November, 2005
DOI: 10.3987/COM-05-S(K)37
Reactions of 1,1-Bis(silylmethyl)-1-alkene with N-Halosuccinimide and Ozone

Jun’ichi Uenishi,* Yusuke Tanaka, Masashi Ohmi, Hotsumi Shimomura, and Nobuyuki Kawai

*Kyoto Pharmaceutical University, Misasagi, Yamashina-ku, Kyoto 607-8412, Japan

Abstract

Electrophilic reactions of 3-phenyl-1,1-bis(trimethylsilymethyl)-1-propene (1) and 1,1-bis[dimethyl(phenyl)silylmethyl]-3-phenyl-1-propene (4) are described. Protodesilylation of 1 with PPTS gave 2-substituted allylsilane (2) in excellent yield. Halogenation of 4 with N-halosuccimide gave a mixture of 3-halo-5-phenyl-2-silylmethyl-1-pentene (5) and 3-halo-5-phenyl-1,2-bis(silylmethyl)-1-pentene (6). The reaction of 1 and 4 with ozone gave no carbonyl compounds but gave 3-hydoxy-5-phenyl-2-silylmethyl-1-pentene (7).

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Note | Special issue | Vol 66, No. 1, 2005, pp.603-610
Published online: 18th October, 2005
DOI: 10.3987/COM-05-S(K)40
Asymmetric Mannich-Type Addition of Lithium Glycolates to Imines Producing 3-Hydroxy-4-phenylazetidin-2-ones

Hiroki Fujieda, Seiji Hata, Ken-ichi Yamada, and Kiyoshi Tomioka*

*Graduate School of Pharmaceutical Sciences, Kyoto University, 46-29 Yoshida-shimoadachi-machi, Sakyo-ku, Kyoto 606-8501, Japan

Abstract

The external chiral ligand-controlled asymmetric Mannich-type reaction of a binary- or ternary-complexed lithium ester enolate of protected glycolates with benzaldehyde imines gave the corresponding 3-trialkylsilyloxy-4-phenylazetidin-2-ones, applicable as a synthetic intermediate of C13 side chain of taxan anticancer drugs, in moderate enantioselectivity.

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Note | Special issue | Vol 66, No. 1, 2005, pp.611-619
Published online: 21st October, 2005
DOI: 10.3987/COM-05-S(K)48
One-Step Synthesis of Ethyl Quinaldates by Lewis Acid Catalyzed Three-Component Coupling Reaction of Aromatic Amines, Aliphatic Aldehydes and Ethyl Glyoxylate

Takashi Inada, Takayuki Nakajima, and Isao Shimizu*

*School of Science and Engineering, Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo 169-8555, Japan

Abstract

A convenient, efficient and simple one-pot method for the synthesis of quinaldates was developed by three-component coupling reaction of an arylamine (1), ethyl glyoxylate and an aliphatic aldehyde (2) in the presence of Lewis acid catalyst. The reaction proceeded most effectively using Yb(OTf)3 as a catalyst.

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Note | Special issue | Vol 66, No. 1, 2005, pp.621-625
Published online: 14th October, 2005
DOI: 10.3987/COM-05-S(K)51
Palladium-catalyzed Cyclocotrimerization of Propargyl Alcohols with Aryl Halides

Shuichi Oi,* Hideki Orihara, Hiroshi Kawai, and Yoshio Inoue*

*Graduate School of Engineering, Tohoku University, Aramaki, Aoba-ku, Sendai 980-8578, Japan

Abstract

Tertiary propargyl alcohols react with aryl halides in the presence of K2CO3 and a catalytic amount of palladium(0) complex affording 2:1 cyclocotrimerization products, 3-benzylidene-2,3-dihydrofuranes (3).

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Note | Special issue | Vol 66, No. 1, 2005, pp.627-637
Published online: 15th November, 2005
DOI: 10.3987/COM-05-S(K)53
Radical Reactions and α-Silylations of Optically Active 4-Trichloromethyl-β-lactone

T. Andrew Mitchell and Daniel Romo*

*Department of Chemistry, Texas A & M University, College Station, Texas 77843-3255, U.S.A.

Abstract

Radical alkylations and α-silylations of optically active (R)-4-trichloromethyl-2-oxetanone are described that maintain the integrity of the β-lactone. Alternate methods for selective dechlorinations of both the β-lactone and the derived Weinreb amide are described.

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Note | Special issue | Vol 66, No. 1, 2005, pp.639-644
Published online: 21st October, 2005
DOI: 10.3987/COM-05-S(K)59
Spiro Crown Ethers Bearing (S)-1,1’-Spirobiindanes as Chiral Backbones

Kohji Yonezawa, Mahesh L. Patil, Hiroaki Sasai, and Shinobu Takizawa*

*The Institute of Scientific and Industrial Research, Osaka University, 8-1, Mihogaoka, Ibaraki, Osaka 567-0047, Japan

Abstract

The synthesis of spiro chiral crown ethers ((S)-1a) and ((S)-1b) has been achieved. The combination of (S)-1a and KOH promoted the asymmetric alkylation of glycine derivative (2) with moderate enantioselectivity.

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Note | Special issue | Vol 66, No. 1, 2005, pp.645-649
Published online: 22nd November, 2005
DOI: 10.3987/COM-05-S(K)62
Hetero-Diels-Alder Reaction Catalyzed by Self-organized Polymeric Rare Earth Complexes under Solvent-free Conditions

Shuichi Ishida, Tetsuji Hayano, Hiroshi Furuno, and Junji Inanaga*

*Synthetic Methodology and Catalysis, Institute for Materials Chemistry and Engineering (IMCE), Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan

Abstract

2-Substituted 2,3-dihydropyran-4-one derivatives were conveniently synthesized under solvent-free conditions by Lewis acid-catalysis with a polymeric scandium sulfonate complex, which can be prepared in a self-organized manner in one step and successfully reused for the next round of reactions.

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Note | Special issue | Vol 66, No. 1, 2005, pp.651-658
Published online: 15th November, 2005
DOI: 10.3987/COM-05-S(K)63
Two New Indole Alkaloids from Aspidosperma subincanum and Geissospermum vellosii

Haruaki Ishiyama, Miyako Matsumoto, Mitsuhiro Sekiguchi, Hideyuki Shigemori, Ayumi Ohsaki, and Jun’ichi Kobayashi*

*Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita 12 Nishi 6, Kita-ku, Sapporo, Hokkaido 060-0812, Japan

Abstract

Two new indole alkaloids, subincanadine G (1) and pausperadine A (2), were isolated from the barks of Aspidosperma subincanum Mart and Geissospermum vellosii Allemão, respectively. Subincanadine G (1) has 1-azoniatricyclo[4.3.3.01,5]undecane moiety, while pausperadine A (2) contains an N-oxide moiety. The gross structures and relative stereochemistry of 1 and 2 were elucidated by spectroscopic data.

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Note | Special issue | Vol 66, No. 1, 2005, pp.659-666
Published online: 28th October, 2005
DOI: 10.3987/COM-05-S(K)64
Synthesis of N-Methylphenanthridinone Derivatives Fused with a Silacyclohexane Ring by Radical Reaction Using Tributyltin Hydride

Yuya Hoshino and Osamu Hoshino*

*Faculty of Pharmaceutical Sciences, Science University of Tokyo, 2641 Yamazaki, Noda, Chiba 278-8510, Japan

Abstract

Radical reaction of (N-methyl-7-bromo-2,2-dimethyl-2-silatetralin-6-ylamino)veratramide (8a) and -piperonamides (8b) in boiling benzene using tributyltin hydride and AIBN gave two kinds of N-methylphenanthridinone derivatives (15 and 16), which were cyclized at 6- and 2-positions of aroylic acid moiety. On the other hand, similar reaction of N-methyl-N-(2-bromoveratryl and 2-bromopiperonyl)-2,2-dimethyl-2-silatetralin-6-carboxamides (14) produced N-methylphenanthridinone deivatives (17) as each sole product, in which cyclization occurred at 5-position of 2-silatetralin moiety.

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Note | Special issue | Vol 66, No. 1, 2005, pp.667-674
Published online: 15th November, 2005
DOI: 10.3987/COM-05-S(K)66
The Structural Information of the Quaternary Ammonium Salts Derived from Nicotine and Sparteine in the Solid State

Kazuhiro Yoshizawa, Yasuko In, Toshimasa Ishida, and Takayuki Shioiri*

*Graduate School of Environmental and Human Sciences, Meijo University, Shiogamaguchi, Tempaku, Nagoya 468-8502, Japan

Abstract

Preparation and X-Ray crystallographic analysis of the benzyl quaternary salts of nicotine and sparteine were described.

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Note | Special issue | Vol 66, No. 1, 2005, pp.675-681
Published online: 29th November, 2005
DOI: 10.3987/COM-05-S(K)69
Are Multicomponent Strecker Reactions of Diketones with Diamines under High Pressure Amenable to Heterocyclic Synthesis?

Koji Kumamoto, Hirokazu Iida, Hiroshi Hamana, Hiyoshizo Kotsuki,* and Kiyoshi Matsumoto,*

*Faculty of Pharmaceutical Sciences, Chiba Institute of Science, 3 Shiomi-cho, Choshi, Chiba 288-0025, Japan

Abstract

Employing double Strecker strategy, two new heterocyclic compounds, 5,6,11,12-tetrahydro-6,11-dimethyldibenzo[b,f][1,4]diazocine-6,11-dicarbonitrile and 1,2,3,4,5,10-hexahydrophenazine-4a,10a-dicarbonitrile, were prepared in one step albeit in low yields. The reaction has proven to be very limited, but such a sterically hindered amine as N-methylaniline underwent Strecker reaction with benzaldehyde and TMSCN to give the corresponding α-amino nitriles.

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Note | Special issue | Vol 66, No. 1, 2005, pp.683-688
Published online: 18th November, 2005
DOI: 10.3987/COM-05-S(K)72
Preparation of N-Sulfonyl-2-quinolinone Using Ring-closing Metathesis (RCM)

Mitsuhiro Arisawa,* Chumpol Theeraladanon, and Atsushi Nishida*

*Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan

Abstract

An efficient method for the preparation of N-sulfonyl-2-quinolinone using ring-closing metathesis (RCM) is described.

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Review | Special issue | Vol 66, No. 1, 2005, pp.689-709
Published online: 4th October, 2005
DOI: 10.3987/REV-05-SR(K)1
Anion Receptors

Oleg N. Chupakhin,* Nadezhda A. Itsikson, Yuri Yu. Morzherin, and Valery N. Charushin

*Institute of Organic Synthesis, Urals Branch, Russian Academy of Sciences, 20, S. Kovalevskaya st., Ekaterinburg, GSP-147, 620219, Russia

Abstract

The review outlines the recent achievements in the field of anion coordination chemistry, and is focusing on the function-oriented design of anion-binding “host” ligands. Comparative analysis of receptor abilities for various classes of organic compounds towards anions is presented.

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Review | Special issue | Vol 66, No. 1, 2005, pp.711-725
Published online: 4th October, 2005
DOI: 10.3987/REV-05-SR(K)2
Enantiotopic Synthesis of Natural Products: Merrilactone and Guanacastepene

Heedong Yun, Zhaoyang Meng, and Samuel J. Danishefsky*

*Department of Chemistry, Columbia University, 3000 Broadway, New York, NY 10027, U.S.A.

Abstract

We have previously disclosed the total syntheses of racemic merrilactone A and guanacastepene A. We describe herein the development of new routes to key intermediates in the first-generation syntheses, which will allow us to access both merrilactone A and guanacastepene A in enantiomerically enriched form.

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Review | Special issue | Vol 66, No. 1, 2005, pp.727-741
Published online: 1st November, 2005
DOI: 10.3987/REV-05-SR(K)3
Synthetic Strategies of Fostriecin

Masakatsu Shibasaki* and Motomu Kanai

*Faculty of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

Abstract

Fostriecin is a naturally occurring triene-containing phosphate ester, which exhibits a potent and selective PP2A inhibitory activity. Due to its interesting chemical structure and biological activity, strategically unique total syntheses of fostriecin were reported from several groups. An overview of the synthesis and chemistry-based structure-activity relationships of fostriecin is described in this review.

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Review | Special issue | Vol 66, No. 1, 2005, pp.743-751
Published online: 15th November, 2005
DOI: 10.3987/REV-05-SR(K)4
Expanding Structural Diversity of Terpene Trilactones from Ginkgo biloba Extract: Studies towards Core-modified Ginkgolides

Sergei V. Dzyuba,* Sergei Bolshakov, Jean Li, and Koji Nakanishi*

*Department of Chemistry, Columbia University, 3000 Boradway, New York, NY 10027, U.S.A.

Abstract

Ginkgolides, the unique terpene trilactones from the Ginkgo biloba tree, are believed to enhance memory, improve blood circulation and exhibit beneficial effects in the treatment of dementia. Unfortunately, mechanisms of ginkgolide actions at the molecular level are still not determined. Ginkgolide skeleton modifications may provide a plausible approach to address subtle changes in the ligand-receptor interactions. Furthermore, the simplified structure of the ginkgolide skeleton may guide to the leads that will be attractive for drug development. This review covers the modifications of the ginkgolide skeleton, reported to date.

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84 data found. 61 - 84 listedFirst Previous