摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

scandine | 73951-55-0

中文名称
——
中文别名
——
英文名称
scandine
英文别名
methyl (1S,10S,12S,19S)-12-ethenyl-9-oxo-8,16-diazapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate
scandine化学式
CAS
73951-55-0
化学式
C21H22N2O3
mdl
——
分子量
350.417
InChiKey
JTSSMMKHJYRYEG-DVWBAYGPSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    58.6
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Alkaloid−Fullerene Systems through Photocycloaddition Reactions<sup>1</sup>
    作者:Li-Wei Guo、Xiang Gao、Dan-Wei Zhang、Shi-Hui Wu、Hou-Ming Wu、Yong-Jiang Li、Stephen R. Wilson、Christine F. Richardson、David I. Schuster
    DOI:10.1021/jo000156h
    日期:2000.6.1
    The photocycloaddition of tertiary amines to [60]fullerene (C-60) is an interesting and useful reaction. We wished to extend the applications of this type of reaction through an investigation of the photoaddition of alkaloids to C-60 for the purpose of synthesizing novel and complex photoadducts that are difficult to obtain by usual methods. Irradiation of tazettine (2) or gramine (3) with Cao in toluene leads to formation of one monoadduct (6 or 7), whereas scandine (1a) or 10-hydroxyscandine (Ib) reacts with C-60 photochemically to give two products, the expected [6,6] monoadduct (5a, 5b) and a new type of monoadduct with a bis-[6, 6] closed structure (4a, 4b). These new structures were characterized by W-vis, FT-IR, H-1 NMR, C-13 NMR, H-1-H-1 COSY, ROESY, HMQC (heteronuclear multiple-quantum coherence), and HMBC (heteronuclear multiple-bond connectivity) spectroscopy. The techniques of time-of-flight secondary ion MS (TOF-SIMS) and field desorption MS (FD-MS) were used for the mass determination. He-3 NMR analysis of the product mixture from photoaddition of la to C-60 containing a He-3 atom (He-3@C-60) led to two peaks at -9.091 and -11.090 ppm relative to gaseous He-3, consistent with formation of a [6,6]-closed monoadduct and a bis-[6,6] closed adduct. Presumably, the bis-[6, 6] closed adducts are formed by an intramolecular [2 + 2] cycloaddition of the vinyl group to the adjacent 6,6-ring junction of C-60 after the initial photocycloaddition.
  • Guo,Li-Wei; Gao, Xiang; Zhang, Dan-Wei, Chemistry Letters, 1999, # 5, p. 411 - 412
    作者:Guo,Li-Wei、Gao, Xiang、Zhang, Dan-Wei、Wu, Shi-Hui、Wu, Hou-Ming、Li, Yong-Jiang
    DOI:——
    日期:——
  • Methyleneindolines, indolenines, and indoleniniums. 20. The first biomimetic synthesis of scandine and meloscine
    作者:Georgette Hugel、Jean Levy
    DOI:10.1021/jo00359a040
    日期:1986.5
查看更多

同类化合物

攀援山橙碱 (+)-(6bR,12aS,12bS,13aS)-12a-(2-hydroxyethyl)-7,8,12a,12b,13,13a-hexahydro-10H-indolizino[1',8'-2,3,4]cyclopenta[1,2-c]quinolin-1(2H)-one methyl (1S,10S,12S,19S)-12-ethenyl-8,16-diazapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2,4,6,8,13-pentaene-10-carboxylate scandine epimeloscine (+)-(6bR,12aS,12bS,13aS)-12a-{2-[(2-nitrophenyl)selanyl]ethyl}-7,8,12a,12b,13,13a-hexahydro-10H-indolizino[1',8'-2,3,4]cyclopenta[1,2-c]quinolin-1(2H)-one meloscine (6bR*,6b(1)S*,12aS*,13aR*)-12a-Vinyl-2,6b(1),7,8,10,12a,13,13a-octahydro-1H-indolizino[1'',8'':2,3,4]cyclopenta[1,2-c]quinolin-1-one Methyl 12-ethenyl-9-oxo-8-aza-16-azoniapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate Methyl 12-ethyl-16-(9-hydroxy-10-methoxycarbonyl-20-methyl-8,16-diazahexacyclo[10.6.1.19,12.01,10.02,7.016,19]icosa-2(7),3,5,13-tetraen-4-yl)-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate Trimethyl 12-hydroxy-6,8-dioxa-11,20-diazahexacyclo[14.6.1.01,13.02,10.05,9.020,23]tricosa-2(10),3,5(9),17-tetraene-11,12,16-tricarboxylate 12-Ethenyl-3-hydroxy-8,16-diazapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2(7),3,5,13-tetraen-9-one 12-Hydroxy-11,12-bis(methoxycarbonyl)-6,8-dioxa-11,20-diazahexacyclo[14.6.1.01,13.02,10.05,9.020,23]tricosa-2(10),3,5(9),17-tetraene-16-carboxylic acid methyl (1S,10R,12S,19S)-12-ethenyl-4-hydroxy-9-oxo-8,16-diazapentacyclo[10.6.1.0^{1,10.0^{2,7.0^{16,19]nonadeca-2(7),3,5,13-tetraene-10-carboxylate Scandin 9-Hydroxy-6-methoxy-8,9-bis(methoxycarbonyl)-8,17-diazapentacyclo[11.6.1.01,10.02,7.017,20]icosa-2(7),3,5,14-tetraene-13-carboxylic acid Methyl 12-acetyl-9-oxo-8,16-diazapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate Methyl 12-ethyl-16-(12-methyl-9,11-dioxo-8,17-diazahexacyclo[11.6.1.110,13.01,10.02,7.017,20]henicosa-2(7),3,5,14-tetraen-4-yl)-14-oxa-8,17-diazahexacyclo[10.7.1.01,9.02,7.013,15.017,20]icosa-2,4,6,9-tetraene-10-carboxylate Methyl 4-(12-ethenyl-10-methoxycarbonyl-9-oxo-8,16-diazapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2,4,6,13-tetraen-15-yl)-12-ethyl-5-hydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9,13-pentaene-10-carboxylate Methyl 4-(12-ethenyl-10-methoxycarbonyl-9-oxo-8,16-diazapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2,4,6,13-tetraen-17-yl)-12-ethyl-5-hydroxy-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,9,13-pentaene-10-carboxylate 12-Methyl-8,17-diazahexacyclo[11.6.1.110,13.01,10.02,7.017,20]henicosa-2,4,6,14-tetraene-9,11-dione 12-Ethenyl-4-hydroxy-10-(2-hydroxyacetyl)-8,16-diazapentacyclo[10.6.1.01,10.02,7.016,19]nonadeca-2(7),3,5,13-tetraen-9-one Meloscin