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(+)-rogioloxepane A | 143120-38-1

中文名称
——
中文别名
——
英文名称
(+)-rogioloxepane A
英文别名
Rogioloxepane A;(2R,7R)-2-[(1R)-1-bromopropyl]-7-[(Z,1R)-1-chlorohex-3-en-5-ynyl]-2,3,6,7-tetrahydrooxepine
(+)-rogioloxepane A化学式
CAS
143120-38-1
化学式
C15H20BrClO
mdl
——
分子量
331.68
InChiKey
ZAQAXRPCNVAIRN-CMEZAIPESA-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):
    5
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:1fe702ef3c360b8d3f8b4ffd20e1c08a
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反应信息

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文献信息

  • The first total synthesis of (+)-rogioloxepane A
    作者:Ryuji Matsumura、Toshio Suzuki、Hisahiro Hagiwara、Takashi Hoshi、Masayoshi Ando
    DOI:10.1016/s0040-4039(00)02281-4
    日期:2001.2
    The first total synthesis of (+)-rogioloxepane A is described. The alpha,omega -trans-disubstituted oxepene skeleton was stereoselectively constructed via cyclization of the hydroxy epoxide promoted by the (Bu3Sn)(2)O/Zn(OTf)(2) system. The proposed configurations of 6R and 13R were confirmed through this synthetic study. (C) 2001 Elsevier Science Ltd. All rights reserved.
  • Enantioselective Total Synthesis of (+)-Rogioloxepane A
    作者:Michael T. Crimmins、Amy C. DeBaillie
    DOI:10.1021/ol034923l
    日期:2003.8.1
    graphicThe enantioselective synthesis of (+)-rogioloxepane A has been achieved in 21 steps from 1,5-hexadien-3-ol. The key steps in the synthesis are an asymmetric glycolate alkylation leading to the diene 2 and a subsequent ring-closing metathesis to construct the oxepene core.
  • On the unusual propensity by the red seaweedLaurencia microcladia of II Rogiolo to form C15 oxepanes: Isolation of rogioloxepane A, B, C, and their likely biogenetic acyclic precursor, prerogioloxepane
    作者:Graziano Guella、Ines Mancini、Giuseppe Chiasera、Francesco Pietra
    DOI:10.1002/hlca.19920750128
    日期:1992.2.5
    It is shown here that the red seaweed Laurencia microcladia KÜTZNING, collected in the Mediterranean off the torrent Il rogiolo, contains the C15 acetogenin rogioloxepane A ( = (+)-(2R,7R)-2-(1-bromopropyl)-7-[(Z)-1-chlorohex-3-en-5-ynyl]-2,3,6,7-tetrahydrooxepin; (+)-3) besides its epoxy derivative rogioloxepane B ((+)-4) and the rogioloxepane C ((+)-5) derived from (+)-4 by epoxide opening. Co-occurring
    在此示出的是,红色海藻凹顶microcladia KÜTZNING,收集在地中海关闭洪流伊尔rogiolo,包含C 15聚乙酸rogioloxepane A(=(+) - (2 R,7 - [R )-2-(1-溴丙基) -7-[( Z )-1-chlorohex-3-en-5-ynyl] -2,3,6,7-tetrahydrooxepin ;(+)- 3)除其环氧衍生物罗戈环庚烷B((+)- 4)外通过环氧化物开环衍生自(+)- 4的rogioloxepane C((+)- 5)。同时出现的是无环C 15产乙酸原素,perrogioloxepane(=(7 R,4 Z,9 Z,12Z)-6-chloropentadeca-3,9,12-trien-1-yn-7-ol; 9),其优选以需要的折叠构象存在,以通过分子内环化产生其偏爱的旋转椅形式的罗格洛环烷A(3TC)。分子力学计算支持这一观点
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