Site-Selective and Nondestructive Protein Labeling through Azaelectrocyclization-Induced Cascade Reactions

被引：36

作者：

Tanaka, Katsunori ^{[1
]}

Fujii, Yohei ^{[1
]}

Fukase, Koichi ^{[1
]}

机构：

[1] Osaka Univ, Grad Sch Sci, Dept Chem, Toyonaka, Osaka 5600043, Japan

来源：

CHEMBIOCHEM | 2008年 / 9卷 / 15期

基金：

日本学术振兴会; 日本科学技术振兴机构;

关键词：

domino reactions; electrocyclic reactions; fluorescent probes; lysine; protein modifications;

D O I：

10.1002/cbic.200800336

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

页码：2392 / 2397

页数：6

共 49 条

[31] Profiling enzyme activities in vivo using click chemistry methods [J].

Speers, AE ;

Cravatt, BF .

CHEMISTRY & BIOLOGY, 2004, 11 (04) :535-546

[32] One-pot and sequential organic chemistry on an enzyme surface to tether a fluorescent probe at the proximity of the active site with restoring enzyme activity [J].

Takaoka, Y ;

Tsutsumi, H ;

Kasagi, N ;

Nakata, E ;

Hamachi, I .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (10) :3273-3280

[33] Nonparabolic valence subband in In0.53Ga0.47As/In0.52Al0.48As multi-quantum wells using transmission Spectroscopy [J].

Tanaka, K. ;

Kotera, N. .

2007 INTERNATIONAL CONFERENCE ON INDIUM PHOSPHIDE AND RELATED MATERIALS, CONFERENCE PROCEEDINGS, 2007, :91-94

[34] Development of highly stereoselective asymmetric 6π-azaelectrocyclization of conformationally flexible linear 1-azatrienes.: From determination of multifunctional chiral amines, 7-alkyl cis-1-amino-2-indanols, to application as a new synthetic strategy:: Formal synthesis of 20-epiuleine [J].

Tanaka, K ;

Kobayashi, T ;

Mori, H ;

Katsumura, S .

JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (18) :5906-5925

[35] Highly stereoselective asymmetric 6π-azaelectrocyclization utilizing the novel 7-alkyl substituted cis-1-amino-2-indanols:: Formal synthesis of 20-epiuleine [J].

Tanaka, K ;

Katsumura, S .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (33) :9660-9661

[36] The inhibitory mechanism of bovine pancreatic phospholipase A2 by aldehyde terpenoids [J].

Tanaka, K ;

Kamatani, M ;

Mori, H ;

Fujii, S ;

Ikeda, K ;

Hisada, M ;

Itagaki, Y ;

Katsumura, S .

TETRAHEDRON, 1999, 55 (06) :1657-1686

[37] Significant acceleration of 6π-azaelectrocyclization resulting from a remarkable substituent effect and formal synthesis of the ocular age pigment A2-E by a new method for substituted pyridine synthesis [J].

Tanaka, K ;

Mori, H ;

Yamamoto, M ;

Katsumura, S .

JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (09) :3099-3110

[38] Synthesis of a new phospholipase A2 inhibitor of an aldehyde terpenoid and its possible inhibitory mechanism [J].

Tanaka, K ;

Kamatani, M ;

Mori, H ;

Fujii, S ;

Ikeda, K ;

Hisada, M ;

Itagaki, Y ;

Katsumura, S .

TETRAHEDRON LETTERS, 1998, 39 (10) :1185-1188

[39] Novel synthesis of the ocular age pigment A2-E: New method for substituted pyridine synthesis via azaelectrocyclization [J].

Tanaka, K ;

Katsumura, S .

ORGANIC LETTERS, 2000, 2 (03) :373-375

[40]

Tanaka K., 2008, ANGEW CHEM, V120, P108

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