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methyl 3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylate | 98678-39-8

中文名称
——
中文别名
——
英文名称
methyl 3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylate
英文别名
2,3-bis(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydronaphthalene;(+/-)-1r-phenyl-1,2,3,4-tetrahydro-naphthalene-dicarboxylic acid-(2t.3t)-dimethyl ester;(+/-)-1r-Phenyl-1,2,3,4-tetrahydro-naphthalin-dicarbonsaeure-(2t.3t)-dimethylester;dimethyl (1R,2S,3R)-1-phenyl-1,2,3,4-tetrahydronaphthalene-2,3-dicarboxylate
methyl 3-(methoxycarbonyl)-1-phenyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylate化学式
CAS
98678-39-8
化学式
C20H20O4
mdl
——
分子量
324.376
InChiKey
NULZFBYAAAVEJZ-KZNAEPCWSA-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):
    3.4
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    250.天然酚醛树脂的成分。第十八部分。1:2:3:4-四氢萘-2:3-二羧酸和1-苯基衍生物
    摘要:
    DOI:
    10.1039/jr9400001321
  • 作为产物:
    参考文献:
    名称:
    3,6-二氢苯并[b] -1,2-草酰-2-氧化物的邻喹啉甲烷
    摘要:
    通过光化学制备的1-羟基-1,3-二氢苯并[b]噻吩-2,从邻甲苯醛中分两步合成3,6-二氢苯并[b] -1,2-草胺-2-氧化物5a,描述了2-二氧化物。还已经进行了苯并亚砜5的3和6个取代衍生物的类似合成。通过在富马酸二甲酯,马来酸二甲酯和巴豆酸甲酯的存在下,以立体定性和高收率在富马酸二甲酯,马来酸二甲酯和巴豆酸甲酯的存在下,在回流环己烷中加热苯基磺胺5c,测试了将这些苯并磺胺类化合物用作邻喹二甲烷前体的可行性。加入马来酸酯的立体化学似乎完全是“ exo”,这与较早的关于α-芳基-o-喹啉二甲烷的Diels-Alder反应的研究相矛盾。
    DOI:
    10.1016/s0040-4039(01)81585-9
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文献信息

  • Stereoselectivity in the Diels-Alder reaction of phenyl- and oxy-substituted o-quinodimethanes
    作者:Tony Durst、Elisabeth C. Kozma、James L. Charlton
    DOI:10.1021/jo00224a035
    日期:1985.11
  • Electrochemical Generation and Reaction of <i>o</i>-Quinodimethanes from {[[2-(2,2-Dibutyl-2-stannahexyl)phenyl]methyl]thio}benzenes
    作者:Madoka Jinno、Yoshikazu Kitano、Masahiro Tada、Kazuhiro Chiba
    DOI:10.1021/ol990647s
    日期:1999.8.1
    The anodic oxidation of [[2-(2,2-dibutyl-2-stannahexyl)phenyl]methyl]thio}benzenes gave o-quinodimethanes which were trapped in situ by dienophiles to give the corresponding cycloadducts in excellent yields. The electron transfer and succeeding 1,4-elimination reaction was efficiently completed in a solution of lithium perchlorate/nitromethane in the presence of acetic acid. The reaction progress was quantitatively controlled by the passage of charge. By using this new method, an aryltetralin lignan skeleton was also synthesized.
  • Jones, David W., Journal of the Chemical Society. Perkin transactions I, 1994, # 4, p. 399 - 406
    作者:Jones, David W.
    DOI:——
    日期:——
  • o-quinodimethanes from 3,6-dihydrobenzo[b]-1,2-oxathiin-2-oxides
    作者:James L. Charlton、Tony Durst
    DOI:10.1016/s0040-4039(01)81585-9
    日期:——
    o-tolual-dehyde via the photochemically produced 1-hydroxy-1,3-dihydrobenzo[b]thiophene-2,2-dioxide is described. Analogous syntheses of 3 and 6 substituted derivatives of the benzosultines 5 have also been carried out. The feasibility of using these benzosultines as o-quinodimethane precursors has been tested by thermalizing the phenyl sultine 5c in refluxing cyclohexane in the presence of dimethyl fumarate, dimethyl
    通过光化学制备的1-羟基-1,3-二氢苯并[b]噻吩-2,从邻甲苯醛中分两步合成3,6-二氢苯并[b] -1,2-草胺-2-氧化物5a,描述了2-二氧化物。还已经进行了苯并亚砜5的3和6个取代衍生物的类似合成。通过在富马酸二甲酯,马来酸二甲酯和巴豆酸甲酯的存在下,以立体定性和高收率在富马酸二甲酯,马来酸二甲酯和巴豆酸甲酯的存在下,在回流环己烷中加热苯基磺胺5c,测试了将这些苯并磺胺类化合物用作邻喹二甲烷前体的可行性。加入马来酸酯的立体化学似乎完全是“ exo”,这与较早的关于α-芳基-o-喹啉二甲烷的Diels-Alder反应的研究相矛盾。
  • 250. The constituents of natural phenolic resins. Part XVIII. 1 : 2 : 3 : 4-Tetrahydronaphthalene-2 : 3-dicarboxylic acid and the 1-phenyl derivative
    作者:Robert D. Haworth、Frank H. Slinger
    DOI:10.1039/jr9400001321
    日期:——
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同类化合物

鬼臼酸哌啶基腙氮氧自由基 鬼臼酸 鬼臼毒醇 苦鬼臼毒醇 米托肼 甘尔布林 珠子草次素 消泡剂 愈创木素 异落叶松脂素 异紫杉脂素9,9'-缩丙酮 异紫杉脂素 大侧柏酸 四环[6.6.2.02,7.09,14]十六烷-2(7),3,5,9(14),10,12-己烯-15,15,16,16-四甲腈 叶下珠新素 五脂素A1 7,8,9,9-四去氢异落叶松树脂醇 7,14-二氢-7,14-乙桥二苯并[a,h]蒽-15,16-二羧酸二钠盐 7,14-二氢-7,14-乙桥二苯并[a,h]蒽-15,16-二甲酸 6,8-二溴-4-氧代-4H-1-苯并吡喃-3-甲醛 5a-苯基-5a,14c-二氢苯并[a]茚并[2,1-c]芴-5,10-二酮 1-苯基-1,2,3,4-四氢-萘-2,3-二羧酸 1-(3,4-二羟基苯基)-6,7-二羟基-1,2-二氢萘-2,3-二甲酸 1-(3,4-二甲氧基苯基)-1,2,3,4-四氢-6,7-二甲氧基-2,3-萘二甲醇 1-(3,4-二甲氧基-苯基)-6,7-二甲氧基-1,2,3,4-四氢-萘-2,3-二羧酸 (7S,8S,9R)-9-(3,4-二甲氧基苯基)-6,7,8,9-四氢-4-甲氧基-7,8-双(甲氧基甲基)萘并[1,2-D]-1,3-二恶茂 (7S,8R,9R)-9-(1,3-苯并二氧戊环-5-基)-7,8-二甲基-6,7,8,9-四氢苯并[g][1,3]苯并二氧戊环 (1S,2R,3S)-1-(3,4-二甲氧基苯基)-1,2,3,4-四氢-6,7-二甲氧基-2,3-二甲基-萘 (11S,12R)-9,10-乙桥-9,10-二氢蒽-11,12-二甲酸 (-)-南烛木树脂酚 (+)-异落叶松脂素 (1RS,2SR)-1,2-dihydro-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxynaphthalene-2,3-dicarboxylic acid dimethyl ester (+/-)-(1R,2S,3R)-12-benzyl-4-hydroxy-6,7-methylenedioxy-1-phenyl-2,3,4-trihydrobenzo[f]isoindol-13-one (+/-)-dimethoxy-epi-isopicropodophyllin N-benzyl lactam (+/-)-(1R,2R,3S)-12-benzyl-6,7-methylenedioxy-4-oxo-1-phenyl-2,3-dihydrobenzo[f]isoindol-13-one (+)-ovafolinin B (5R,6R)-methyl 7-(6-fluoro-1H-benzo[d]imidazol-2-yl)-5-(3,4,5-trimethoxyphenyl)-5,6-dihydronaphtho[2,3-d][1,3]dioxole-6-carboxylate 2,5,8-trimethoxy-4a,9,9a,10-tetrahydro-9,10-[1,2]benzenoanthracene-1,4-dione 2,11-dichloro-13b-phenylbenzo[a]indeno[1,2-c]fluorene-9,14(8bH,13bH)-dione rel-(1R,4aR,9S,9aS,10R)-4a,9,9a,10-tetrahydro-9,10-diphenylspiro[9,10-epoxyanthracene-1(4H),2'-oxiran]-4-one 1,4-diphenyl-1,2,3,4-tetrahydro-1,4-epoxido-naphthalene-2,3-dicarboxylic acid diethyl ester rel-(1R,4aS,9R,9aS,10S)-4a,9,9a,10-tetrahydro-9,10-diphenylspiro[9,10-epoxyanthracene-1(4H),2'-oxetane]-4-one endo-2,5-diphenyl-3,4-benzo-14-oxatetracyclo<7.2.2.12,5.01,6>tetradec-3-ene 1a,2,7,7a-tetrahydro-2,7-epoxy-1a-methyl-1,2,7-triphenylbenzonaphthothiophenium triflate endo-2,5-diphenyl-3,4-benzo-14-oxatetracyclo<6.3.2.12,5.01,6>tetradec-3-ene (1S,8R,9S,10S)-1,8-diphenyl-10-methyl-11-oxa-tricyclo[6.2.1.02,7]undeca-2(7),3,5-triene-9-carboxaldegyde 13b-phenylbenzo[a]indeno[1,2-c]fluorene-9,14(8bH,13bH)-dione (1R,2R)-7-methyl-1,2,3-tris(4-methylphenyl)-1,2-dihydronaphthalene methyl 9-deoxy-9-oxo-α-apopicropodophyllate 9-n-hexylimine (15R)-13-(4-fluorophenyl)-10-hydroxy-10,11-dihydro-9H-9,10-[3,4]epipyrroloanthracene-12,14(13H,15H)-dione