Regular Issue

Vol. 2, No. 1, 1974

17 data found. 1 - 17 listed
Communication | Regular issue | Vol 2, No. 1, 1974, pp.1-4
Published online:
DOI: 10.3987/R-1974-01-0001
Molecular Design by Cycloaddition Rections. XIII. Cycloaddition of 1,3-Diphenylisobenzofuran with cis-Bicyclo[6.1.0]nona-2,4,6-triene

Tadashi Sasaki,* Ken Kanematsu, and Yusaku Yukimoto

*Institute of Applied Organic Chemistry, Faculty of Engineering, Nagoya University, Chikusa, Nagoya, Aichi 464-8601, Japan

Abstract

Cycloaddition reaction of 1,3-diphenylisobenzofuran with cis-bicyclo[6.1.0]nona-2,4,6-triene gave four 1 : l adducts. The structural elucidation of major products was accomplished by spectral evidences and chemical properties. Possible mechanism for the reaction is also discussed.

PDF (87KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.5-7
Published online:
DOI: 10.3987/R-1974-01-0005
Reissert Compound Studies. Part XXV. A Novel Reaction with 2-Nitrobenzaldehyde and the Anion of 2-Acetyl-1,2-dihydroisoquinaldonitrile

Harry W. Gibson and Frank D. Popp*

*Department of Chemistry, Clarkson College of Technology, Potsdam, New York 13676, U.S.A.

Abstract

In contrast to the reaction of the anion of 2-benzoyl-1,2-dihydroisoquinaldonitrile with aldehydes, the reaction of the anion of 2-acetyl-1,2-dihydroisoquinaldonitrile with 2-nitrobenzaldehyde involves the formation of a novel type of product (VII).

PDF (45KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.9-14
Published online:
DOI: 10.3987/R-1974-01-0009
A Synthesis of Benzocarbazole Derivatives by Thermolysis

Tetsuji Kametani,* Toshio Suzuki, Kimio Takahashi, and Keiichiro Fukumoto

*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan

Abstract

A thermal reaction of indolylmagnesium bromide (1) with 1- cyano-4,5-dimethoxybenzocyclobutene (2) gave a mixture of 6-cyano-5a,6,11,11a-tetrahydro-8,9-dimethoxy-5H-benzo[b]carbasole (3a) and 6-cyano-5a,6,11,11a-tetrahydro-9-hydroxy-8-methaxy-5H-benzo[b]carbazole (4). Compound (3a) was easily converted to 6-cyano-8,9-dimethoxy-5H-benzo[b]carbazole (6) by dehydrogenation on 30 % Pd-C.

PDF (85KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.15-19
Published online:
DOI: 10.3987/R-1974-01-0015
Synthesis of a Non-Saccharical Analog of Puromycin

Frans M. Kaspersen, Hans Bieräugel, and Upendra K. Pandit*

*Organic Chemistry Laboratory, University of Amsterdam, Nieuwe Achtergracht 129, 1018 WS Amsterdam, The Netherlands

Abstract

The synthesis of (2S,4S)-N-(p-methoxyphenyl-L-alanyl)-2-hydroxymethyl-4-[N9-6- (dimethylamino)purinyl]pyrrolidine (1), a non-saccharidal analog of puromycin, is described.

PDF (104KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.21-26
Published online:
DOI: 10.3987/R-1974-01-0021
Cyclization of β-Ketosulfoxide. IV. Synthesis of Indole, Benzothiophene and Carbazole Derivatives

Yuji Oikawa, Osamu Setoyama, and Osamu Yonemitsu*

*Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan

Abstract

On acid-treatment, β-ketosulfoxides having pyrrole, thiophene and indole nuclei were converted to indoles, benzothiophenes and carbazoles, respectively, through intramolecular nucleophilic substitution.

PDF (91KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.27-32
Published online:
DOI: 10.3987/R-1974-01-0027
Studies of Polyazapentalenes. V. The Cycloaddition Reaction of 8-Methyldibenzo[b,e]-1,3a,6a-triazapentalene with Asymmetrical Acetilenes

Otohiko Tsuge* and Hideo Samura

*Research Institute of Industrial Science, Faculty of Engineering, Kyushu University, 6-1, Kasuga-koen, Kasuga 816-8580, Japan

Abstract

Triazapentalene (I) reacted with asymmetrical acetylenes (II) to give the corresponding [3+2] cycloadducts as major products. It has been found that phenyl- and p-chlorophenylacetylene added to I in different directions, and that methyl phenylpropiolate gave two [3+2] cycloadducts.

PDF (110KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.33-37
Published online:
DOI: 10.3987/R-1974-01-0033
The Stereochemistry of (±)-6a-β-Ethyl-1,2,5,6,6a,7,8,9,9a-α,9b-α-decahydro-4H-pyrrolo[3,2,1-i,j]quinolin-9β-ol

Kyoyu Sasaki, Yuji Sendo, Masao Akagi, and Yoshio Ban*

*Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060-0812, Japan

Abstract

The methiodide(V) of the entitled compound was submitted to X-ray analysis, and the structure was established to be the one shown in Fig. 1, which is represented by the formula (V).

PDF (87KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.39-43
Published online:
DOI: 10.3987/R-1974-01-0039
Derivatives of 1,2-Dithiole-3-thiones. III. A Novel Desulfurization of 4,5-Benzo-1,2-dithiole-3-thione Imide or Its Selemium Analogue

Seizo Tamagaki, Keishi Sakaki, and Shigeru Oae*

*Department of Chemistry, University of Tsukuba, 1-1-1 Ten-nodai, Tsukuba-shi, Ibaraki, 305-8571, Japan

Abstract

N-Benzenesulfonylimide of 4,5-benzo-1,2-dithiole-3-thione(C=35S) was thermally desulfurized to afford a corresponding 3-(N-benzenesulfonyl)imine with predominant extrusion of the exocyclic thiono sulfur atom, while with its selenium analogues, the exclusive loss of thiolo sulfur instead of exocyclic selenium atom was observed, resulting in the formation of the selenium-migrating product, i.e., 4,5-benzo-1,2-thiaselenole-3-(N-benzenesulfonyl)imine.

PDF (82KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.45-50
Published online:
DOI: 10.3987/R-1974-01-0045
Derivatives of 1,2-Dithiole-3-thiones. IV. Oxidation of 4,5-Benzo-3-selenoxo-1,2-dithiole

Seizo Tamagaki, Keishi Sakaki, and Shigeru Oae*

*Department of Chemistry, University of Tsukuba, 1-1-1 Ten-nodai, Tsukuba-shi, Ibaraki, 305-8571, Japan

Abstract

The desulfurizative oxidation of 1,2-dithiole-3-thiones with various oxidizing reagents was reexamined using 4,5-benzo-3-selenoxo-1,2-dithiole as a typical substrate. The product thus obtained was 4,5-benzo-1,2-thiaselenole-3-one, but not an expected 4,5-benzo-1,2-dithiole-3-one. The reaction pathway via a selenine1 is postulated.

PDF (91KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.51-54
Published online:
DOI: 10.3987/R-1974-01-0051
Photodehydroxylation of Some 3-Hydroxyoxindoles

Noboru Shoji, Yoshikazu Kondo,* and Tsunematsu Takemoto

*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan

Abstract

Photoreduction of 3-substituted 3-hydroxyoxindoles I-IV in the presence of sodium hydrosulfite led to loss of the 3-hydroxyl group. Irradiation at longer wavelengths (λ> 3000 Å) did not cause this photodehydroxylation.

PDF (60KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.55-59
Published online:
DOI: 10.3987/R-1974-01-0055
Total Synthesis of (±)-Mecambridine

Tetsuji Kametani,* Akira Ujiie, and Keiichiro Fukumoto

*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan

Abstract

Hydroxymethylation of the phenolic tetrahydroprotoberberine (VII) yielded O-demethylmecambridine (VIII), which on methylation with diazomethane afforded (±)-mecambridine (XII). This work proved the structure of this base to be 7,8 ,13,14-tetrahydro-12-hydroxymethyl-1 ,10,11-trimethoxy-2,3-methylenedioxyprotoberberine.

PDF (103KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.61-66
Published online:
DOI: 10.3987/R-1974-01-0061
Semisynthetic β-Lactam Antibiotics. V. Synthesis of α-Sulfobenzylpenicillin by Using Mixed Anhydride and Active Ester of α-Sulfophenylacetic Acid

Shiro Morimoto,* Hiroaki Nomura, Toshihiro Ishiguro, Takeshi Fugono, and Kihachiro Maeda

*Central Research Division, Takeda Chemical Industries, Ltd., 17-85 Jusohonmachi 2-chome, Yodogawa-ku, Osaka 532-8686, Japan

Abstract

The synthesis of α-sulfobenzylpenicillin (V) was first accomplished in our Research Laboratory. The compound exhibits the peculiar activity against G(+) and G(-) bacteria. For the preparation of this penicillin several activated derivatives of α-sulfophenylacetic acid (I) have been obtained in the purified form.

PDF (71KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.67-72
Published online:
DOI: 10.3987/R-1974-01-0067
Semisynthetic β-Lactam Antibiotics. VII. New Semisynthetic Cephalosporins Derived from α-Sulfhenylacetic Acid

Hiroaki Nomura,* Takeshi Fugono, Takenori Hitaka, Isao Minami, Toshiyuki Azuma, Shiro Morimoto, and Toru Masuda

*Central Research Division, Takeda Chemical Industries, Ltd., 17-85 Jusohonmachi 2-chome, Yodogawa-ku, Osaka 532-8686, Japan

Abstract

The preparation of derivatives of α-sulfophenylacetic acid has been made from 7-aminocephalosporanic acid. New semisynthetic cephalosporins exhibit a peculiar inhibitory effect against Pseudomonas aeruginosa.

PDF (77KB)
Communication | Regular issue | Vol 2, No. 1, 1974, pp.73-78
Published online:
DOI: 10.3987/R-1974-01-0073
Studies on Vinca Alkaloids. The Structure of Vincarodine

James P. Kutney,* Gloria Cook, James Cook, Isamu Itoh, Jon Clardy, Jose Fayos, Peter Brown, and Gordon H. Svoboda

*Department of Chemisry, University of British Columbia, Vancouver 8, V5T 1W5, Canada

Abstract

The structure and stereochemistry of vincarodine (1) have been determined by an investigation of its spectroscopic properties, particularly NMR, electron impact and field ionization mass spectrometry and finally by X-ray analysis of the hydrobromide derivative.

PDF (90KB)
Review | Regular issue | Vol 2, No. 1, 1974, pp.79-103
Published online:
DOI: 10.3987/R-1974-01-0079
Synthesis of Pentazocine

Tetsuji Kametani,* Kazuo Kigasawa, Mineharu Hiiragi, and Nagatoshi Wagatsuma

*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan

Abstract

Synthetic studies of pentazocine and its intermediates are described and classified.

PDF (383KB)
Review | Regular issue | Vol 2, No. 1, 1974, pp.105-123
Published online:
DOI: 10.3987/R-1974-01-0105
Application of Enamide Photocyclization to the Synthesis of Natural Products

Ichiya Ninomiya*

*Kobe Women’s College of Pharmacy, Motoyamakita, Higashinad, Kobe, Hyogo 658, Japan

Abstract

Enamide photocyclization has been shown to be a new and useful tool for the synthesis of various nitrogen-containing heterocyclic systems, particularly alkaloids. By this means, the synthesis of crinan, benzo(c)phenanthridine, aporphine, protoberberine and yohimbine alkaloids has been achieved.

PDF (292KB)
Review | Regular issue | Vol 2, No. 1, 1974, pp.125-152
Published online:
DOI: 10.3987/R-1974-01-0125
Concerting the Biosynthesis of Vitamin B12

A. Ian Scott*

*Sterling Chemistry Laboratory, Yale University, 225 Prospect St., New Haven, CT 06511, U.S.A.

Abstract

The use of 13C FT-NMR has led to the observation that while 8 molecules of [2-13C] -ALA are incorporated into vitamin B12 in P. shermanii, [5-13C]-ALA labels only seven of the carbon atoms of cyanocobalamin i.e. one of the amino methyl groups of ALA is “lost” in the process. It has also been confirmed that seven of the methyl groups of B12 are derived from 13CH3 enriched methionine and further that the chirality of the gem-dimethyl grouping at C12 labeled with [13CH3]-methionine is R. A soluble enzyme mixture from the 37,000 g supernatant of disrupted cells of P. shermanii converts both 14C-labeled ALA and 14C-uro’gen III to cobyrinic acid, the simplest corrinoid material on the pathway to vitamin B12 and the coenzyme in presence of NADPH, Co++ , Mg++, S-adenosylmethionine and glutathione. A detailed hypothesis of the mechanism of corrin synthesis from uro’gen III has been developed.

PDF (513KB)
17 data found. 1 - 17 listed