The Structures of Gardnerine, Gardnutine and Hydroxygardnutine and the Absolute Configuration of Gardnerine
スポンサーリンク
概要
- 論文の詳細を見る
Four kinds of indole alkaloids, gardneramine, gardnerine, gardnutine and hydroxygardnutine, were isolated from Gardneria nutans SIEB. et ZUCC. (Horaikazura). Among them, gardnerine, gardnutine and hydroxygardnutine were examined and the structures, I, II and III were assigned respectively to gardnerine, gardnutine and hydroxygardnutine on the basis of chemical and physical data. The main alkaloid gardnerine (I) was interrelated with ajmaline (IV)(of established absolute configuration) by two different routes (A and B). In the route A, I was transformed to 1-demethyl-Δ^1-17,21-dideoxyajmaline (XXVIII) which in turn was erived from ajmaline (IV). On the other hand, in the route B, I was transformed to XXXII which in turn was derived from isoajmaline (XXXV)(C_<20>-ethyl epimer of ajmaline). The stereochemistry of the ethylidene side chain of II was determined by NOE measurement. These correlations as well as the nuclear overhauser effect (NOE) experiment established the absolute stereochemistry of I, II and III as shown in Chart 15.
- 社団法人日本薬学会の論文
- 1973-08-25
著者
-
坂井 進一郎
Faculty of Pharmaceutical Sciences, Chiba University
-
久保 陽徳
Meiji College of Pharmacy
-
高橋 勝弘
Department of Antibiotics, Research Institute for Chemobiodynamics, Chiba University
-
高橋 勝弘
Department Of Antibiotics Research Institute For Chemobiodynamics Chiba University
-
萩庭 丈寿
千葉大学薬学部
-
大谷 裕之
千葉大学薬学部
-
久保 陽徳
Faculty of Pharmaceutical Sciences, Chiba University
-
浜本 武紀
Faculty of Pharmaceutical Sciences, Chiba University
-
若林 幹夫
Faculty of Pharmaceutical Sciences, Chiba University
-
高橋 勝弘
Faculty of Pharmaceutical Sciences, Chiba University
-
大谷 裕之
Faculty of Pharmaceutical Sciences, Chiba University
-
萩庭 丈寿
Faculty of Pharmaceutical Sciences, Chiba University
-
坂井 進一郎
Faculty Of Pharmaceutical Sciences Chiba University
-
若林 幹夫
Faculty Of Pharmaceutical Sciences Chiba University
-
浜本 武紀
Faculty Of Pharmaceutical Sciences Chiba University
関連論文
- New Corymine-Related Indole Alkaloids from Hunteria zeylanica in Thailand
- A NEW CLASS OF TWO DIMERIC INDOLE ALKALOIDS, CORYZEYLAMINE AND DEFORMYLCORYZEYLAMINE, FROM THE LEAVES OF HUNTERIA ZEYLANICA IN THAILAND
- Novel Indole Alkaloids from the Leaves of Rauwolfia sumatrana JACK. in Thailand
- HUNTERIOSIDE, FIRST BIOSE BOUND MONOTERPENOID INDOLE ALKALOID FROM HUNTERIA ZEYLANICA
- Two New Dimeric Indole Alkaloids from Tabernaemontana subglobosa MERR. from Taiwan
- A Nuclear Magnetic Resonance Study on the Eleven Stereoisomers of Heteroyohimbine-Type Oxindole Alkaloids
- KINGINOSIDE, A NEW ACYL GROUP CARRYING IRIDOID BIOSIDE FROM LONICERA MORROWII
- The Structure of Garcinone E
- On the Alkaloidal Constituents of Aconitum sanyoense NAKAI var. tonense NAKAI
- SYNTHESIS OF LYALOSIDE, A PROTOTYPAL β-CARBOLINE GLUCO INDOLE ALKALOID IN RUBIACEOUS PLANTS
- STRUCTURES OF TWO NEW BITTER PRINCIPLES ISOLATED FROM A THAI MEDICINAL PLANT, VERNONIA EXTENSA D. C.
- FIVE NEW NAPELLINE-TYPE DITERPENE ALKALOIDS FROM ACONITUM LIANGSHANIUM
- Partial Synthesis of Rauwolfia Alkaloids, Vomilenine and (19Z)-Vomilenine, and Their Relative Thermodynamic Stability as Revealed by Their Transformation into Perakine
- STRUCTURE AND SYNTHESIS OF TWO NEW TYPES OF OXINDOLE ALKALOIDS FOUND FROM UNCARIA SALACCENSIS
- TWO NEW DITERPENE ALKALOIDS, 10-HYDROXYISOTALATIZIDINE AND 10-HYDROXY-TALATIZAMINE
- Synthesis of Saframycins. X. Transformation of (-)-Saframycin A to (-)-Saframycin Mx Type Compound with the Structure Proposed for Saframycin E
- Synthesis of Saframycins. VIII. Synthesis of the ABC Ring of Safracins
- SYNTHESIS OF SAFRAMYCINS. VI. THE USEFUL TRANSFORMATION OF (-)-SAFRAMYCIN A TO (-)-SAFRAMYCIN Mx TYPE COMPOUND
- SYNTHESIS OF SAFRAMYCINS. IV. : SELENIUM OXIDE OXIDATION OF 4-OXO-HEXAHYDRO-1,5-IMINO-3-BENZAZOCIN-7,10-DIONE; PROMISING METHOD TO CONSTRUCT SAFRAMYCINS C AND D FROM SAFRAMYCIN B
- A Facile Synthesis of 1,2,3,4-Tetrahydroisoquinolines through Cyclization of O, N-Acetals. II. : Syntheses of Isoquinolinequinone Antibiotics
- Synthssis of Saframycins. II. : Preparations and Reactions of N-Methyl-2,5-piperazinediones
- Preparations and Reactions of (Z)-3-Arylidene-6-arylmethyl-2,5-piperazinediones Having Highly Oxygenated Benzene Rings(Organic,Chemical)
- STRUCTURE OF SAFRAMYCIN D, A NEW DIMERIC ISOQUINOLINEQUINONE ANTIBIOTIC(Communications to the Editor)
- Synthesis of 1,2,3,4,5,8-Hexahydroisoquinoline-5,8-diones Using Oxidative Demethylation with Ceric Ammonium Nitrate or Argentic Oxide
- The Structures of Gardnerine, Gardnutine and Hydroxygardnutine and the Absolute Configuration of Gardnerine
- 10 ホウライカヅラアルカロイド類の絶対配置について
- THE STRUCTURE AND ABSOLUTE CONFIGURATION OF HANAMISINE
- THE STRUCTURE AND ABSOLUTE CONFIGURATION OF SADOSINE
- THE STRUCTURE OF IGNAVINE
- 55 新抗生物質Saframycin A,B,Cの構造
- Synthesis of 5,6-, 5,8- and 7,8-Isoquinolinediones from the Corresponding Isoquinolinols and Dimethoxyisoquinolines
- STRUCTURE OF TWO NEW DITERPENE ALKALOIDS, 3-EPI-IGNAVINOL AND 2,3-DEHYDRODELCOSINE
- GARDNERIA ALKALOIDS PART 14. THE STRUCTURE OF GARDFLORAMINE AND 18-DEMETHOXYGARDFLORAMINE(Communications to the Editor)
- HYDROLYTIC DEGRADATION OF β-CARBOLINE-TYPE MONOTERPENOID GLUCOINDOLE ALKALOIDS : A POSSIBLE MECHANISM FOR HARMAN FORMATION IN Ophiorrhiza AND RELATED RUBIACEOUS PLANTS
- Studies on Plants containing Indole Alkaloids. VIII Indole Alkaloid Glycosides and Other Constituents of the Leaves of Uncaria rhynchophylla MIQ.
- PARTIAL SYNTHESIS OF DIHYDROTHYSANOLACTONE
- Structure Elucidation of a New Aconite Alkaloid, 15-α-Hydroxyneoline
- THE STRUCTURES OF ADDITIONAL TELEOCIDIN CLASS TUMOR PROMOTERS
- The Synthesis of Secamine and Presecamine Skeletons and the Isolation of Tetrahydrosecamine from Amsonia elliptica ROEM et SCHULT.
- Reactions of Indole Related Compounds. III. (E) and (Z)-2-Oxoindolin-3-ethylidenes
- SYNTHESIS OF SAFRAMYCINS. I. TOTAL SYNTHESIS OF (±)-SAFRAMYCIN B AND ITS CONGENERS.(Communication to the Editor)
- Studies on Plants containing Indole Alkaloids. VI. Minor Bases of Uncaria rhynchophylla MIQ.
- The C2-C3 Bond Cleavage Reaction of Indole Alkaloids
- THE PREPARATION OF 14-HYDROXYLATED YOHIMBINE AND RESERPINE DERIVATIVES
- Dioxopyrrolines. XXXII. X-Ray Determination of the Molecular Structure of a Photoadduct of 2-Trimethylsilyloxybutadiene to 3-Ethoxycarbonyl-2-phenyl-Δ^2-pyrroline-4,5-dione
- SYNTHESIS OF MERIDINE, A PENTACYCLIC AZA-AROMATIC ALKALOID
- Synthesis of 8-Amino-5,6-quinolinediones from 6-Quinolinols and 5,6-Dimethoxyquinolines
- Synthesis of New Isoquinolinequinone Metabolites of a Marine Sponge, Xestospingia sp., and the Nudibranch Jorunna funebris
- Synthesis of Mimocin, an Isoquinolinequinone Antibiotic from Streptomyces lavendulae, and Its Congeners
- Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids
- Structure of Gardneramine and 18-Demethylgardneramine
- インドールアルカロイド類の転換反応(第2報)インドールアルカロイドのC/D環開環ならびに閉環反応とVobasine型アルカロイドの合成について
- 37 インドールアルカロイド類の転換反応 : C/D環,開環並びに閉環反応について
- Oxidation of 2,3-Disubstituted Indole Derivatives with Selenium Dioxide
- 13 Gardneria属塩基Gardneramineの構造
- Gardneria Alkaloids(第5報) : Sarpagine骨核のC, D環開裂反応
- Gardneria Alkaloids(第4報) : Gardneria nutans SIEB.et ZUCC.(ホウライカズラ), G.Multiforia MAKINO(チトセカズラ), G.Shimadai HAYATA(タイワンチトセカズラ)ならびにいわゆるG.Insularis NAKAI(エイシュウカズラ)の塩基成分比較
- Studies on the N-Oxides of π-Deficient N-Heteroaromatics. XIII. Mass Spectra of Azanaphthalene N-Oxides and Their Photochemical Reaction Products
- 含窒素環状化合物の新合成法(第14報) : 1,2,3,5,6,6a, 7,8,9,9a-Decahydropyrido[2,1,6-de]quinolizine誘導体の合成
- ホウライカヅラ(Gardneria nutans SIEB.et ZUCC.)のアルカロイド
- A Novel Skeletal Rearrangement of Aromatic N-Oxides upon Electron Impact
- 5,6-Dihydro-pyrrolo[2,1-a]isoquinoline類の合成
- Pictet-Spengler法によるアセタールカルボン酸エステル類とトリプタミンの縮合
- 3 ホウライカヅラ(Gardneria nutans Sieb. et Zucc.)よりのIndole系アルカロイド
- Decahydropyrido [2,1,6-de] quinolizine (Decahydrocycl [3.3.3] azine)
- Indole系アルカロイド含有植物の検索その4Ochrosia nakaiana KOIDZ.(ヤロード)の塩基成分
- Indole系アルカロイド含有植物の検索その1 : Uncaria属植物塩基について
- ELUCIDATION OF THE STRUCTURES OF OLIVORETIN B AND C
- SYNTHESIS OF OPTICALLY ACTIVE TELEOCIDIN DERIVATIVES. ABSOLUTE CONFIGURATION OF TELEOCIDIN B AND OLIVORETIN A
- ELUCIDATION OF THE STRUCTURE OF OLIVORETIN A AND D (TELEOCIDIN B)
- A New Indole Alkaloid, 14α-Hydroxyrauniticine : Structure Revision and Partial Synthesis
- A Convenient Synthesis of 1,2,3,4,6,7,12,12b-Octahydroindolo-[2,3-α]quinolizine Derivatives
- Transformation of Indole Alkaloids. VI. A Novel Conversion of Oxindole Alkaloids into Indole Alkaloids via Indoline Derivatives
- Synthesis of Renierone, 7-Methoxy-1,6-dimethyl-5,8-dihydroisoquinoline-5,8-dione and N-Formyl-1,2-dihydrorenierone, Antimicrobial Metabolites from a Marine Sponge, Reniera sp.
- SYNTHESIS OF ISOQUINOLINEQUINONE ANTIBIOTICS FROM A MARINE SPONGE Reniera sp.
- Synthesis of 4,7-Indolequinones. The Oxidative Demethylation of 4,7-Dimethoxyindoles with Ceric Ammonium Nitrate
- The Assignment of the Carbon-13 Nuclear Magnetic Resonance Spectra of Isoquinoline and Quinoline Quinones
- THE CERIC AMMONIUM NITRATE MEDIATED SYNTHESIS OF QUINOLINE AND ISOQUINOLINE QUINONES
- THE CONVERSION OF PSEUDOKOBUSINE TO KOBUSINE
- THE STRUCTURE OF THE NEW DITERPENE ALKALOID NOMININE AND THE ABSOLUTE CONFIGURATION OF KOBUSINE
- THE STRUCTURE OF A NEW DITERPENE ALKALOID : SANYONAMINE
- THE STRUCTURE OF HYPOGNAVINE
- THE PARTIAL SYNTHESIS OF ISODELPHININE
- The Partial Synthesis of Heteroyohimbine Alkaloids : Akuammigine, 3-Isorauniticine and Corynanthe Alkaloid ; Corynantheidine
- A New Synthesis of Dihydromancunine
- Transformation of Indole Alkaloids. The Chemical Transformation of Corynantheine Type Alkaloids to C-Mavacurine Type Alkaloids
- Asymmetric Synthesis and Absolute Configuration of (-)-Trypargine
- ASYMMETRIC SYNTHESIS OF (1S)-(-)-TRYPARGINE
- Synthesis of Renierone, Antimicrobial Metabolite from a Marine Sponge Reniera sp.
- Studies on Plants containing Indole Alkaloids. VII. Isolation of Several Aspidosperma-and Vincamine-type Alkaloids from the seeds of Amsonia elliptica ROEM. et SCHULT.
- A REARRANGEMENT OF AN ASPIDOSPERMA TYPE ALKALOID INTO A TETRAHYDROQUINOLINE DERIVATIVE : UNAMBIGUOUS CONFIRMATION OF THE RESULTING SKELETON STRUCTURE
- Synthetic Sutdies on the Picraline-Type Indole Alkaloids-I : Improved Synthesis of C-Mavacurine-Type Compounds and a New Skeletal Rearrangement in a Corynanthe-Type Derivative
- ISOLATION AND STRUCTURE ELUCIDATION OF TELEOCIDIN B-1,B-2,B-3,AND B-4
- A Convenient Synthesis of 1,2,3,4,6,7,12,12b-Octahydroindolo-[2,3-a] quinolizine
- Imidazo{2,1-b]benzothiazoles. II. : Synthesis and Antinflammatory Activity of Some Imidazo[2,1-b]benzothiazoles
- Imidazo[2,1-b]benzothiazoles. I
- The Chemical Transformation of Gardnerine to 2-Acylindole Alkaloid"Ochropine"
- INDOLE ALKALOIDS ISOLATED FROM GELSEMIUM ELEGANS(THAILAND) : 19-(Z)-AKUAMMIDINE, 16-EPI-VOACARPINE, 19-HYDROXYDIHYDRO-GELSEVIRINE, AND THE REVISED STRUCTURE OF KOUMIDINE(Communications to the Editor)
- 4,4-Dimethyl Effect. (5). The Conformation of 8αH, 14βH-Onocerane-3,21-dione (Onoceranedione-I) in the Crystalline State