TANNINS AND RELATED-COMPOUNDS .106. PREPARATION OF AMINOALDITOL DERIVATIVES OF HYDROLYZABLE TANNINS HAVING ALPHA-GLUCOPYRANOSE AND BETA-GLUCOPYRANOSE CORES, AND ITS APPLICATION TO THE STRUCTURE ELUCIDATION OF NEW TANNINS, REGININ-A AND REGININ-B AND FLOSIN-A, ISOLATED FROM LAGERSTROEMIA-FLOS-REGINAE RETZ
文献类型:期刊论文
作者 | XU, YM; SAKAI, T; TANAKA, T; NONAKA, G; NISHIOKA, I |
刊名 | CHEMICAL & PHARMACEUTICAL BULLETIN
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出版日期 | 1991-03 |
卷号 | 39期号:3页码:639-646 |
关键词 | HYDROLYZABLE TANNIN AMINOALDITOL DERIVATIVE REGININ-A REGININ-B FLOSIN-A LAGERSTROEMIN VALONEIC ACID LAGERSTROEMIA-FLOS-REGINAE LYTHRACEAE TANNIN |
ISSN号 | 0009-2363 |
文献子类 | Article |
英文摘要 | To avoid tautomerism in the hydrolyzable tannins which lack an acyl group at the glucose C-1 position, a new method for the protection of the C-1 atom has been developed. That is reaction of the tannins with p-anisidine in the presence of acetic acid, followed by sodium cyanoborohydride reduction, afforded, without notable hydrolysis of ester bonds, the aminoalditol derivatives (1a-7a) in 50-80% yields. The proton and carbon-13 nuclear magnetic resonance (H-1- and C-13-NMR) spectra of these derivatives exhibited much simpler signal patterns typical of an open-chain form of glucose, and almost all the signals could be assigned. Application of this method to the structure elucidation of the new tannins, flosin A (22) and reginins A (23) and B (24), isolated from the leaves of Lagerstroemia flos-reginae RETZ. (Lythraceae), established their structures including the orientation of the 4,6-positioned valoneoyl group. In addition, the structure of a new hydrolyzable tannin, lagerstroemin (21), which was concomitantly isolated from the above species, was elucidated. |
WOS关键词 | ELLAGITANNINS |
WOS研究方向 | Pharmacology & Pharmacy ; Chemistry |
语种 | 英语 |
WOS记录号 | WOS:A1991FF26900019 |
出版者 | PHARMACEUTICAL SOC JAPAN |
源URL | [http://119.78.100.183/handle/2S10ELR8/275207] ![]() |
专题 | 中国科学院上海药物研究所 |
作者单位 | 1.CHINESE ACAD SCI, SHANGHAI INST MAT MED, SHANGHAI, PEOPLES R CHINA 2.KYUSHU UNIV 62, FAC PHARMACEUT SCI, 3-1-1 MAIDASHI, HIGASHI KU, FUKUOKA 812, JAPAN |
推荐引用方式 GB/T 7714 | XU, YM,SAKAI, T,TANAKA, T,et al. TANNINS AND RELATED-COMPOUNDS .106. PREPARATION OF AMINOALDITOL DERIVATIVES OF HYDROLYZABLE TANNINS HAVING ALPHA-GLUCOPYRANOSE AND BETA-GLUCOPYRANOSE CORES, AND ITS APPLICATION TO THE STRUCTURE ELUCIDATION OF NEW TANNINS, REGININ-A AND REGININ-B AND FLOSIN-A, ISOLATED FROM LAGERSTROEMIA-FLOS-REGINAE RETZ[J]. CHEMICAL & PHARMACEUTICAL BULLETIN,1991,39(3):639-646. |
APA | XU, YM,SAKAI, T,TANAKA, T,NONAKA, G,&NISHIOKA, I.(1991).TANNINS AND RELATED-COMPOUNDS .106. PREPARATION OF AMINOALDITOL DERIVATIVES OF HYDROLYZABLE TANNINS HAVING ALPHA-GLUCOPYRANOSE AND BETA-GLUCOPYRANOSE CORES, AND ITS APPLICATION TO THE STRUCTURE ELUCIDATION OF NEW TANNINS, REGININ-A AND REGININ-B AND FLOSIN-A, ISOLATED FROM LAGERSTROEMIA-FLOS-REGINAE RETZ.CHEMICAL & PHARMACEUTICAL BULLETIN,39(3),639-646. |
MLA | XU, YM,et al."TANNINS AND RELATED-COMPOUNDS .106. PREPARATION OF AMINOALDITOL DERIVATIVES OF HYDROLYZABLE TANNINS HAVING ALPHA-GLUCOPYRANOSE AND BETA-GLUCOPYRANOSE CORES, AND ITS APPLICATION TO THE STRUCTURE ELUCIDATION OF NEW TANNINS, REGININ-A AND REGININ-B AND FLOSIN-A, ISOLATED FROM LAGERSTROEMIA-FLOS-REGINAE RETZ".CHEMICAL & PHARMACEUTICAL BULLETIN 39.3(1991):639-646. |
入库方式: OAI收割
来源:上海药物研究所
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