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Chinese Journal of Organic Chemistry 2002 Vol.22
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Chin. J. Org. Chem. 2002, 22 (1): 0-.
Published: 25 January 2002
Abstract
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205
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283
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Organic reactions mediated by low-valent vanadium reagents and their applications in organic synthesis
Fan Xuesen;Zhang Yongmin;Zhang Yongmin
Chin. J. Org. Chem. 2002, 22 (1): 1-10.
Published: 25 January 2002
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2334
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Some organic reactions mediated by low-valent vanadium reagents and their applications in organic synthesis are reviewed with an emphasis on the carbon-carbon bond formation reactions such as reuctive coupling of alkyl halides, reductive coupling of aldehydes and ketones, deoxygenative alkylation and deoxygenatie coupling of carbonyl compounds. Those reactions that are mediated by catalytic amounts of low-valent vanadium reagents are given special attention.
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Cited: Baidu(
11
)
Enzymatic synthesis of non-natural oligosaccharides
Cao Hongzhi;Li Zuyi
Chin. J. Org. Chem. 2002, 22 (1): 11-21.
Published: 25 January 2002
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2499
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Enzymes are indispensable tools in modern organic synthesis. Progress in cloning techniques, microbiology and protein purification has been supplying an ever-growing number and quantity of preparatively useful biocatalysts. Initially enzymes were only used to synthesize compounds found in nature. Nowadays they are also used on non-natural substrates under mild and environment-friendly conditions. In general enzymatic synthese have the advantage of excellent chemo-, regio- and stereo-selectivities. The present article focuses on the applicatio of glycosyltransferases in the area of molecular glycobiology. Selected reactions with non-natural substrates are discussed.
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Cited: CSCD(
4
)
Recent developments in the asymmetric synthesis of optically active 2-arylpropanonic acids
Chen Zhilong;Wu Yulin;Wu Yikang
Chin. J. Org. Chem. 2002, 22 (1): 22-32.
Published: 25 January 2002
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2235
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This paper summarized the main asymmetric synthetic methods for optically active 2-arylpropanonic acids as non-steroidal anti- inflammatory agents, especialy for Ibuprofen and Naproxen.
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A review of near-infrared laser protective dyes
Yang Xiaobing;Ding Songtao;Yang Yusheng;Zhou Xiaohai
Chin. J. Org. Chem. 2002, 22 (1): 33-41.
Published: 25 January 2002
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2760
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Due to the requirement of near-infrared laser protective dyes and laser stealth materials, this review focused on the research progress of near-infrared absorbing dyes, and some suggestions were put forward on the future research. Some of the most important technical requiremnets for laser-protective dyes with in the plastic are as follows: sharp absorption bands at specific wavelengths corresponding to laser emission, excellent lightfastness, robust thermal and chemical stability, stability to ambient conditions, high optical density and scotopic luminous transmission, good solubility in plastic and low toxicity. This review paid attention to the properties such as the maximum absorption wavelength and the absorption intense, attention had been directed towards eight types near-infrared dyes: cyanine dyes which included polymethine dyes and squarylium or croconium dyes, phthalocyanines and naphthalocyanines, metal complex dyes, quinone dyes, azo dyes, radical dyes, multiphenylmethane dyes and perylene dyes. Other kinds of near- infrared dyes were also mentioned, such as aromatic annulenes, planes containign so-called nonbenzenoid aromatic rings, cyclic cross- conjugated hydrocarbons having inserted p-quiniod ring, fluorenylium dyes with inorganic anions, donor-acceptor cyclophanes, tetrapyrazinoporphyrazines and pentaazadentate expanded porphyrins et al. All of the dyes mentioned above had some good properties for use as the near-infrared laser protective dyes and laser stealth materials, but there also existed defects in every kind of dyes.
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Cited: Baidu(
44
)
Enantioselective syntheiss of chiral 1-ferrocenyl alcohol via CBS- reduction
Chen Weiyi;Lu Jun;Zhang Yawen;Shen Zongxuan
Chin. J. Org. Chem. 2002, 22 (1): 42-45.
Published: 25 January 2002
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2414
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Reduction of prochiral ferrocenyl ketones (2a~2e) in the presence of 10 mol% of chiral β-amino alcohols(4a~4c) provides 1-ferrocenyl alcohols(1a~1e) in high yields(>85%) with high optically purity(ee up to 96%).
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Relationship between ^13C NMR chemical shifts of alkanes and ionicity index and polarizability effect index
Nie Changming;Li Zhonghai;Wen Songnian
Chin. J. Org. Chem. 2002, 22 (1): 46-51.
Published: 25 January 2002
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2216
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The atomic ionicity index in a molecule has been defined and the model of ^13C NMR chemical shifts of alkanes has been studied with the atomic ionicity index (INI), polarizability effect index (PEI) and the structural information parameters N^i~H(i=αβΥ). The results indicate that the ^13C NMR chemical shifts of alkanes can be described as follows: CS= 194.6156-37.7394(INI)+98.6505(ΣPEI)+27. 1630(INI/ΣPEI)- 652.9106(ΣPEI/INI)+0.7735N^ α~H+2.2468N^β~H- 0. 1742N^γ~H. The chemical shifts of 304 carbon atoms are predicted with the standard error being only 0.9860δ and the average absolute error 0.77 δ. The calculated values are well consistent with the observed ones.
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Improvements on the synthesis of the minor components of the aggregation pheromone of the west indian sugarcane borer
Li Yan;Tian Juan;Huang Jinxia
Chin. J. Org. Chem. 2002, 22 (1): 52-55.
Published: 25 January 2002
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1924
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Both enantiomers of 2-methyl-4-heptanol and 2-methyl- 4-octanol, the minor components of the aggregatio pheromone produced by th emale and female West Indian sugarcane borer (Metamasius hemipterus), have been synthesized starting from natural product (S)-leucine. The key step is preparation of (2R) and (2S)-4-methyl-1, 2-oxidopentane from (2S)- 4-methyl-entane- 1, 2-diol. The optical purity of the target products is over 95%.
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Synthesis and properties of diethylferrocenyl ferrocenyl methanols and their amine derivatives
Li Baoguo;Gao Daiwei;Cao Lizhi;Zhao Wei
Chin. J. Org. Chem. 2002, 22 (1): 56-59.
Published: 25 January 2002
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2035
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Reduction of 1, 1'-diethyl-2(and 3)-ferrocenoylferrocenes with LiAlH4 gave corresponding diferrocenylmethanols, which were very sensitive to acid. These methanols were treated with BF3 in CH2Cl2 to generate the diferrocenylmethyl carbocations. Without separation from the reaction mixture, the ions were treated with some amines RNH2 [R=C2H5, n-C3H7, n-C4H9, HOCH2CH2, HOCH(CH3)CH2, HOCH2CH(C2H5)] to afford the ferrocenylamines in high yields. The present methodology for preparing α-ferrocenylamines from α-ferrocenyl alcohols enjoys such advantages as simple procedure and inexpensive starting materials.
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Enantiomeric resolution of secondary aromatic alcohols and arylethanediols by HPLC on chiral stationary phase
Xia Lijun;Tang Minhua;Hu Jianbing;Ding Zuoding;Jin Hao;Zhao Gang
Chin. J. Org. Chem. 2002, 22 (1): 60-63.
Published: 25 January 2002
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2416
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Separation of racemic mixtures of thirty-eight secondary aromatic alcohols and arylethanediols with different substituting group was achieved with HPLC by using Chiralcel OD and Chiralcel LJ as chiral stationary phase and hexane/2-propanol mixtures of different ratios as eluents. The chromatographic parameters of these racemates on OD and OJ columns were examined. The results showed enantiomeric resolution ability of the racemic mixtures on these columns was strongly dependent on the site and the property of substituents. The hydrogen bonding and π-π interactions between the chiral stationary phase and the polar group o secondary aromatic alcohols and arylethanediols may be responsible for the chiral resolution. This method had been applied to determination of the optical purity of the asymmetric reduction products of prochiral ketones.
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Cited: Baidu(
12
) CSCD(
6
)
Asymmetric reduction of chiral titanium complexes of α-keto aromatic acids with lithium dialkyl amides
Duan Xinfang;Yin Chenglie
Chin. J. Org. Chem. 2002, 22 (1): 64-66.
Published: 25 January 2002
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2510
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Chiral titanium complexes of α-keto aromatic acids(2), obtained by introducing chiral alkoxyligands into titanium complexes of the keto acids, were reduced by lithium dialkyl amides(3) yielding the corresponding mandelic acids in 8.3 to 24.9% ee.
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New compounds against aphides from stellera chamaejasme L.
Hou Taiping;Cui Qiu;Chen Shuhua;Hou Ruotong;Liu Shigui
Chin. J. Org. Chem. 2002, 22 (1): 67-70.
Published: 25 January 2002
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2125
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Two compounds that display high bioactivity against aphides were isolated for the first time from the roots of Stellera chamaejasme L. . Their structures were identified on the basis of various spectral data including IR, UV, NMR, GC-MS and elemenal analysis. They are 1, 5-diphenyl-1-pentanone and 1, 5-diphenyl-2-penten-1-one.
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Cited: CSCD(
18
)
Ionic liquids catalyzed one-pot synthesis of 3, 4-dihydropyrimidin-2 (1H)-ones
Peng Jiajian;Deng Youquan
Chin. J. Org. Chem. 2002, 22 (1): 71-73.
Published: 25 January 2002
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2361
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908
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Dihydropyrimidinones and their derivatives were synthesised in high yields by a one-pot threecomponent Biginelli condensation in th epresence of catalytic amounts of room temperature ionic liquids such as 1-n-Butyl- 3-methylimidazolium tetrafluoroborate (BMImBF4) and hexafluorophosphorate (BMImPF6) under neurtral and solvent-free conditions. The one-pot Biginelli condensation has such advantages as high-yields, short reaction time, and simple procedure.
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Chin. J. Org. Chem. 2002, 22 (10): 0-.
Published: 25 October 2002
Abstract
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224
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(259KB)(
306
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Coupling reaction of aryl halides or triflates with amines catalyzed by palladium and other transition metal
Zhang Zhenfa;Zhou Weicheng
Chin. J. Org. Chem. 2002, 22 (10): 685-693.
Published: 25 October 2002
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2425
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(362KB)(
1338
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Cited: Baidu(
48
) CSCD(
9
)
Progresses in the fluorination addition reactions of unsaturated carbon-carbon bonds
Chen Xinbing;An Zhongwei
Chin. J. Org. Chem. 2002, 22 (10): 694-701.
Published: 25 October 2002
Abstract
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1956
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(317KB)(
2266
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Cited: Baidu(
1
)
Synthesis and properties of chiral calixarenes
Tian Zhenfeng;Zheng Yansong
Chin. J. Org. Chem. 2002, 22 (10): 702-709.
Published: 25 October 2002
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2052
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(324KB)(
913
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Cited: Baidu(
4
) CSCD(
2
)
Application of peroxidase in asymmetric oxidation and the reaction mechanism
Fang Weishuo;Cheng Kedi
Chin. J. Org. Chem. 2002, 22 (10): 710-717.
Published: 25 October 2002
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2220
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(252KB)(
895
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Cited: Baidu(
11
) CSCD(
8
)
Recent progress of the synthetic study on sialic acid (n- acetylneuaminic acid) and its analogs
Li Liansheng;Liu Kegang;Yao Zhujun;Wu Yulin
Chin. J. Org. Chem. 2002, 22 (10): 718-734.
Published: 25 October 2002
Abstract
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2371
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(666KB)(
1267
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Cited: CSCD(
9
)
Research development of ionic organotin compounds
Song Xueqing;Zhong Guiyun;Huang Yanqin;Xie Qinglan
Chin. J. Org. Chem. 2002, 22 (10): 735-740.
Published: 25 October 2002
Abstract
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2383
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(219KB)(
820
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Cited: CSCD(
5
)
Synthesis of 2-methyl-3-aryl-7-(5,5-dimethyl-3-one-1-cyclohexenyl-1- yl)-formyloxy-4(3h)-quinazolinones
Luo Tiejun;Li Zhengming;Zhao Weiguang;Fan Zhijin
Chin. J. Org. Chem. 2002, 22 (10): 741-745.
Published: 25 October 2002
Abstract
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2082
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(166KB)(
616
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Cited: CSCD(
8
)
Syntheses and characterization of mono-substituted calix [6] arenes derivatives
Yang Fafu;Chen Yuanyin;Lin Shen
Chin. J. Org. Chem. 2002, 22 (10): 746-749.
Published: 25 October 2002
Abstract
(
1990
)
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(123KB)(
816
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Cited: Baidu(
12
)
Synthesis of isopropyl salicylate using microwave irradiation
Li Yuntian;Yin Yingwu
Chin. J. Org. Chem. 2002, 22 (10): 750-753.
Published: 25 October 2002
Abstract
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2126
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(117KB)(
753
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Cited: Baidu(
13
) CSCD(
2
)
Synthesis and activity of glycoprotein IIb/IIIa antagonist
Zhang Hong;Guo Zongru
Chin. J. Org. Chem. 2002, 22 (10): 754-760.
Published: 25 October 2002
Abstract
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2086
)
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(243KB)(
531
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Cited: Baidu(
1
)
Synthesis of 5,6-dehydronorcantharidin derivatives of susbstituted aromatic amine and their anti-tumor activities
Liu Fulong;Jiang Tao;Zuo Daishu;Qi Xin;Zhan Xiaolin
Chin. J. Org. Chem. 2002, 22 (10): 761-767.
Published: 25 October 2002
Abstract
(
1945
)
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(244KB)(
835
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Cited: CSCD(
6
)
Aromatization and crystal structure of diether 4-aryl-2,6-dimethyl- 1,4-dihydropyridine-3,5-dicarboxylate under microwave irradiation
Feng Youjian;Gao Yuan;Zhou Jianfeng;Tu Shujiang;Shi Daqing
Chin. J. Org. Chem. 2002, 22 (10): 768-772.
Published: 25 October 2002
Abstract
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2205
)
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(170KB)(
519
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Cited: Baidu(
98
) Baidu(
90
) CSCD(
1
)
Synthesis of bishydroxyl tetracoordinate silicon
Song Jianhua;Zhang Yonghua;Liu Anhua;Gong Kecheng
Chin. J. Org. Chem. 2002, 22 (10): 773-777.
Published: 25 October 2002
Abstract
(
1944
)
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(152KB)(
781
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Cited: Baidu(
13
) CSCD(
9
)
High pressure synthesis of nitrophenylamines type nonlinear optical compounds
Zou Xinzhuo;Toshikaz Ibata
Chin. J. Org. Chem. 2002, 22 (10): 778-781.
Published: 25 October 2002
Abstract
(
2004
)
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(123KB)(
698
)
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Cited: Baidu(
1
)
Solvent-free synthesis of 2-substituted benzimidazoles under microwave-irradiation using PPA as a catalyst
Lu Jun;Ge Hongguang;Bai Yinjuan
Chin. J. Org. Chem. 2002, 22 (10): 782-784.
Published: 25 October 2002
Abstract
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2476
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(105KB)(
834
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Cited: Baidu(
129
) CSCD(
23
)
Synthesis and characterization of 1-aroyl-4-aryl hydrazinecarboxyamides
Li Laizhong;Guo Dianshun;Liu Qingjian;Xu Kehua
Chin. J. Org. Chem. 2002, 22 (10): 785-787.
Published: 25 October 2002
Abstract
(
2013
)
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(102KB)(
643
)
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Cited: Baidu(
10
) CSCD(
6
)
Catalysis of the biginelli reaction by NiCl_2·6H_2O-one-pot synthesis of 3,4-dihydropyrimidin-2(1h)-ones
Lu Jun;Wang Feili;Bai Yinjuan;Li Wanhua
Chin. J. Org. Chem. 2002, 22 (10): 788-792.
Published: 25 October 2002
Abstract
(
2710
)
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(170KB)(
587
)
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Cited: CSCD(
7
)
Study on the reaction of 6-alkoxy-tetrachloro-12h-dibenzo [d,g][1,3, 2]-dioxaphosphocin-6-sulfides with DMSO
Zhang Xiaomei;Yang Daibin;Wang Daoquan;Chen Wanyi
Chin. J. Org. Chem. 2002, 22 (10): 793-796.
Published: 25 October 2002
Abstract
(
1998
)
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(175KB)(
433
)
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Synthesis, characterization and crystal structure of one- dimensional chain polymer chlorodibenzyltin piperazinylmonodithiocarbamate with S…S and S…Cl interactions
Yin Handong;Wang Chuanhua;Ma Chunlin;Wang Yong;Zhang Rufen
Chin. J. Org. Chem. 2002, 22 (10): 797-800.
Published: 25 October 2002
Abstract
(
2000
)
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(149KB)(
339
)
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Cited: CSCD(
2
)
Chin. J. Org. Chem. 2002, 22 (11): 0-.
Published: 25 November 2002
Abstract
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182
)
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(272KB)(
267
)
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Recent advances in organic reactions using zinc metal as reductant
Li Guoping;Jiang Huanfeng;Li Jinheng
Chin. J. Org. Chem. 2002, 22 (11): 801-806.
Published: 25 November 2002
Abstract
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2560
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(213KB)(
3943
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This paper reviews the advances in studies of various reactions using zinc metal as reductant in the presence of catalysts, including the reduction of carbon-carbon multiple bonds, crabon-oxygen double bonds, carbon-nitrogen bonds, carbon-oxygen bonds, carbon-sulfur bonds and carbon-halide bonds.
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Cited: CSCD(
3
)
Recent development in asymmetric synthesis of
Ma Zhihua;Zhao Yonghua;Wang Jianbo
Chin. J. Org. Chem. 2002, 22 (11): 807-816.
Published: 25 November 2002
Abstract
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2255
)
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(450KB)(
1334
)
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Cited: Baidu(
13
) CSCD(
2
)
Advances in the synthesis of glycosphingolipids
Zhu Feng;Wu Xiongyu;Lin Yongcheng
Chin. J. Org. Chem. 2002, 22 (11): 817-826.
Published: 25 November 2002
Abstract
(
1932
)
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(400KB)(
1681
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The total syntheses of sphingosine, ceramide and glycosphingolipid were reviewed with emphasis on the recent progresses.
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Cited: Baidu(
18
) CSCD(
8
)
Progress in hydrolysis of carboxylic esters using artifical enzymes cyclodextrins
Cao Feng;Ren Yong;Hua Weiyi;Ma Kunfang;Guo Yinlong
Chin. J. Org. Chem. 2002, 22 (11): 827-834.
Published: 25 November 2002
Abstract
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2298
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1356
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Cyclodextrins have been playing important roles in the artifical enzymes because of their special structures and characters. This article reviews the progress in hydrolysis of carboxylic esters using simple cyclodextrins, cyclodextrins with catalytic group and cyclodextrin dimmers.
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Cited: CSCD(
6
)
Advances in studies on phosphorylation of polysaccharides
Chen Xiaoming;Tian Gengyuan
Chin. J. Org. Chem. 2002, 22 (11): 835-839.
Published: 25 November 2002
Abstract
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2121
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1430
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This paper reviews the recent progress in phosphate of saccharide and the methods of preparing their derivative.
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Cited: Baidu(
54
) CSCD(
7
)
Recent advances in asymmetric catalysis using 1,1'-bi-2-naphthol
Li Xiaoyong;Nie Jin
Chin. J. Org. Chem. 2002, 22 (11): 840-852.
Published: 25 November 2002
Abstract
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1894
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Optically active 1,1'-bi-2-naphthol has been extensively studied as an excellent chiral ligand in asymmetric catalysis. This review describes recent advances in the applications of monomeric and polymeric binaphthols in a variety of catalytic asymmetric reactions. Several new catalytic strategies involving 1,1'-bi-2-naphthol ligand are also highlighted.
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Cited: CSCD(
4
)
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