LAMPTEROMYCES BIOLUMINESCENCE .5. CHEMICAL SYNTHESIS OF LAMPTEROFLAVIN AS MUSHROOM LIGHT EMITTER

被引：10

作者：

ISOBE, M

TAKAHASHI, H

GOTO, T

机构：

[1] Laboratory of Organic Chemistry, School of Agriculture, Nagoya University Chikusa, Nagoya

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 05期

关键词：

D O I：

10.1016/S0040-4039(00)94611-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Lampteroflavin was synthesized through coupling between 5-trityl-2,3-(p-methoxy)benzylidene-1-β-D-ribofuranosyl trichloacetimidate and 2′,4′-(p-methoxy)benzylidene derivative of riboflavin to produce the crucial alpha riboside. Chloroethyl group was removed under neutral condition. © 1990.

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页码：717 / 718

页数：2

相关论文

共 9 条

[1] LAMPTEROMYCES BIOLUMINESCENCE .2. LAMPTEROFLAVIN, A LIGHT EMITTER IN THE LUMINOUS MUSHROOM, LAMPTEROMYCES-JAPONICUS [J].

ISOBE, M ;

UYAKUL, DC ;

GOTO, T .

TETRAHEDRON LETTERS, 1988, 29 (10) :1169-1172

[2]

Isobe M, 1987, J Biolumin Chemilumin, V1, P181, DOI 10.1002/bio.1170010306

[3] SYNTHESIS OF ALTERNATE LINEAR AND BRANCHED REPEATING UNITS OF THE ESCHERICHIA-COLI LP-1092 CAPSULAR POLYSACCHARIDE CONTAINING "3-DEOXY-ALPHA-D-MANNO-2-OCTULOSONIC ACID (KDO) LINKED TO SECONDARY POSITIONS OF D-RIBOSE [J].

KOSMA, P ;

CHRISTIAN, R ;

SCHULZ, G ;

UNGER, FM .

CARBOHYDRATE RESEARCH, 1985, 141 (02) :239-253

[4]

MIKHAILOV SN, 1984, CA 7016T, V102

[5] HIGHLY STEREOSELECTIVE SYNTHESIS OF ALPHA-RIBONUCLEOTIDES VIA A CYCLIC PHOSPHATE [J].

MUKAIYAMA, T ;

HAYASHI, Y ;

HASHIMOTO, Y .

CHEMISTRY LETTERS, 1985, (07) :1087-1090

[6] SYNTHETIC STUDIES ON CELL-SURFACE GLYCANS .54. A TOTAL SYNTHESIS OF HEMATOSIDE, ALPHA-NEUGC-(2-]3)-BETA-GAL-(1-]4)-BETA-GLC-(1-]1)-CER [J].

NUMATA, M ;

SUGIMOTO, M ;

SHIBAYAMA, S ;

OGAWA, T .

CARBOHYDRATE RESEARCH, 1988, 174 :73-85

[7] NEW METHODS FOR THE SYNTHESIS OF GLYCOSIDES AND OLIGOSACCHARIDES - ARE THERE ALTERNATIVES TO THE KOENIGS-KNORR METHOD [J].

SCHMIDT, RR .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1986, 25 (03) :212-235

[8]

UYAKUL D, 1990, IN PRESS TETRAHEDRON

[9]

UYAKUL D, 1989, IN PRESS BIOORGANIC