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4-amino-4-deoxy-2,3-di-O-tert-butyldimethylsilyl-5,6:7,8-di-O-isopropylidene-D-erythro-L-altro-octono-1,4-lactam | 874350-58-0

中文名称
——
中文别名
——
英文名称
4-amino-4-deoxy-2,3-di-O-tert-butyldimethylsilyl-5,6:7,8-di-O-isopropylidene-D-erythro-L-altro-octono-1,4-lactam
英文别名
5,6:7,8-O-diisopropylidene-2,3-di-O-tert-butyldimethylsilyl-D-erythro-L-altro-octono-γ-lactam;(3R,4S,5S)-3,4-bis[[tert-butyl(dimethyl)silyl]oxy]-5-[(4R,5S)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-1,3-dioxolan-4-yl]pyrrolidin-2-one
4-amino-4-deoxy-2,3-di-O-tert-butyldimethylsilyl-5,6:7,8-di-O-isopropylidene-D-erythro-L-altro-octono-1,4-lactam化学式
CAS
874350-58-0
化学式
C26H51NO7Si2
mdl
——
分子量
545.864
InChiKey
KJEJUYGSPMKJST-WCAYHLDQSA-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):
    4.94
  • 重原子数:
    36
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    84.5
  • 氢给体数:
    1
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Isolation synthesis and glycosidase inhibition profile of 3-epi-casuarine
    摘要:
    3-epi-Casuarine, the first naturally occurring stereoisomer of casuarine, was isolated from Myrtus communis L. The glycosidase inhibition profile and NMR spectra of 3-epi-casuarine are compared with those of casuarine; the change in configuration at one of the six stereogenic centres causes a dramatic change in the conformation of the bicyclic system. The key step in the 6% overall yield synthesis of 3-epi-casuarine from D-gluconolactone is the efficient cyclization of a completely unprotected pentahydroxyaminomcsylate to the pyrrolizidine nucleus. A low yield synthesis of casuarine is also reported. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2006.10.005
  • 作为产物:
    描述:
    (R)-4-Amino-2,3-dihydroxy-4-((4S,5R,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-yl)-butyric acid methyl ester 在 咪唑 作用下, 以 四氢呋喃甲苯 为溶剂, 反应 3.0h, 生成 4-amino-4-deoxy-2,3-di-O-tert-butyldimethylsilyl-5,6:7,8-di-O-isopropylidene-D-erythro-L-altro-octono-1,4-lactam
    参考文献:
    名称:
    Isolation synthesis and glycosidase inhibition profile of 3-epi-casuarine
    摘要:
    3-epi-Casuarine, the first naturally occurring stereoisomer of casuarine, was isolated from Myrtus communis L. The glycosidase inhibition profile and NMR spectra of 3-epi-casuarine are compared with those of casuarine; the change in configuration at one of the six stereogenic centres causes a dramatic change in the conformation of the bicyclic system. The key step in the 6% overall yield synthesis of 3-epi-casuarine from D-gluconolactone is the efficient cyclization of a completely unprotected pentahydroxyaminomcsylate to the pyrrolizidine nucleus. A low yield synthesis of casuarine is also reported. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2006.10.005
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文献信息

  • [EN] SYNTHESIS OF POLYHYDROXYLATED ALKALOIDS<br/>[FR] SYNTHÈSE DES ALCALOÏDES POLYHYDROXYLÉS
    申请人:MNL PHARMA LTD
    公开号:WO2006008493A1
    公开(公告)日:2006-01-26
    A process for the production of a polyhydroxylated bicyclic (e.g. pyrrolizidine such as casuarine (10), indolizidine or quinolizidine) alkaloid comprises the cyclisation of a pyrrolidine or piperidine intermediate having three or more free hydroxyl groups.
    一种用于生产多羟基双环(例如吡咯里西啶,例如相思豆碱(10)、吲哚里西啶或喹诺里西啶)生物碱的过程,包括将具有三个或更多自由羟基的吡咯烷或哌啶中间体进行环合。
  • Isolation synthesis and glycosidase inhibition profile of 3-epi-casuarine
    作者:Jeroen Van Ameijde、Graeme Horne、Mark R. Wormald、Raymond A. Dwek、Robert J. Nash、Paul Wyn Jones、Emma L. Evinson、George W.J. Fleet
    DOI:10.1016/j.tetasy.2006.10.005
    日期:2006.10
    3-epi-Casuarine, the first naturally occurring stereoisomer of casuarine, was isolated from Myrtus communis L. The glycosidase inhibition profile and NMR spectra of 3-epi-casuarine are compared with those of casuarine; the change in configuration at one of the six stereogenic centres causes a dramatic change in the conformation of the bicyclic system. The key step in the 6% overall yield synthesis of 3-epi-casuarine from D-gluconolactone is the efficient cyclization of a completely unprotected pentahydroxyaminomcsylate to the pyrrolizidine nucleus. A low yield synthesis of casuarine is also reported. (c) 2006 Elsevier Ltd. All rights reserved.
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