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1,2-dibenzoyl-3,4-diphenyl-cyclobutane | 33415-81-5

中文名称
——
中文别名
——
英文名称
1,2-dibenzoyl-3,4-diphenyl-cyclobutane
英文别名
1,2-Dibenzoyl-3,4-diphenyl-cyclobutan;(2-Benzoyl-3,4-diphenylcyclobutyl)-phenylmethanone
1,2-dibenzoyl-3,4-diphenyl-cyclobutane化学式
CAS
33415-81-5
化学式
C30H24O2
mdl
——
分子量
416.519
InChiKey
WCTIPYXJFUKGBD-UHFFFAOYSA-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):
    6.2
  • 重原子数:
    32
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    氯化苄 以8%的产率得到
    参考文献:
    名称:
    GEOKUYAN G. G.; TOROSYAN G. O.; BABAYAN A. T., AJKAKAN KIMIAKAN AMSAGIR, ARM. XIM. ZH., 1981, 34, HO 1, 34-39
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • CYCLOADDITION REACTIONS USING QUANTUM DOTS
    申请人:Northwestern University
    公开号:US20200331836A1
    公开(公告)日:2020-10-22
    Disclosed herein are methods in which colloidal quantum dots (QDs) can serve as visible-light chromophores, photocatalysts, and reusable scaffolds for homo- and hetero-intermolecular [2+2] photocycloadditions. The methods may lead to >90% tunable regioselectivity and up to 98% diastereoselectivity for previously minor syn-cyclobutane products, including the syn-head-to-tail cyclobutane.
    本文公开了一种利用胶体量子点(QDs)作为可见光色团、光催化剂和同、异分子[2+2]光环加成的可重复支架的方法。该方法可能导致>90%的可调节区域选择性和高达98%的对映选择性,包括以前较小的同构环丁烷产物,包括同向头尾环丁烷
  • Cycloaddition reactions using quantum dots
    申请人:Northwestern University
    公开号:US10961178B2
    公开(公告)日:2021-03-30
    Disclosed herein are methods in which colloidal quantum dots (QDs) can serve as visible-light chromophores, photocatalysts, and reusable scaffolds for homo- and hetero-intermolecular [2+2] photocycloadditions. The methods may lead to >90% tunable regioselectivity and up to 98% diastereoselectivity for previously minor syn-cyclobutane products, including the syn-head-to-tail cyclobutane.
    本文公开了胶体量子点(QDs)可作为可见光发色团、光催化剂和可重复使用的支架,用于同分子和异分子间[2+2]光环加成反应的方法。这些方法可使以前次要的合成环丁烷产物(包括合成头尾环丁烷)的可调区域选择性大于 90%,非对映选择性高达 98%。
  • Stobbe; Bremer, Journal fur praktische Chemie (Leipzig 1954), 1929, vol. <2> 123, p. 15
    作者:Stobbe、Bremer
    DOI:——
    日期:——
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同类化合物

二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基](1S,2S,3R,4S)-3,4-二(苯基)环丁烷-1,2-二羧酸酯 二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基](1S,2R,3S,4R)-3,4-二(苯基)环丁烷-1,2-二羧酸酯 r-1,t-2-二甲基-t-3,c-3,4-二苯基环丁烷 r-1,t-2,c-3-三苯基-c-4-氰基环丁烷 3,4-双(4-羟基苯基)环丁烷-1,2-二羧酸 3,4-二苯基环丁烷-1,2-二羧酸 1-甲氧基-4-(2,2,3,3-四甲基环丙基)苯 1-[2,3-二甲基-4-(2,4,5-三甲氧基苯基)环丁基]-2,4,5-三甲氧基苯 (2,3,4-三苯基环丁基)苯 (1R,2S,3S,4R)-3,4-二(苯基)环丁烷-1,2-二甲酸二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基]酯 4,9-bis(2-methoxyphenyl)-3a,4,9,9a-tetrahydro-1H-4,9-epoxybenzo[f]isoindole-1,3(2H)-dione (2S,3R)-1-(Hydroxy-phenyl-methyl)-2,3-diphenyl-4-[1-phenyl-meth-(E)-ylidene]-cyclobutanol 2,3,5,6-Tetraphenyl-1,4-cyclohexandion (1S,2S,3S,4S)-3,4-Bis-[2-(di-p-tolyl-phosphinoyl)-phenyl]-cyclobutane-1,2-dicarboxylic acid diethyl ester endo-1,2-dicarbomethoxy-5,5-dimethyl-exo-3,4-diphenylbicyclo<2.1.0>pentane 2-Methylen-3,4-dihydroxy-trans-5,6-diphenylbicyclo<3.1.0>hexan 1,1,4,4-Tetramethyl-2,3b,5,6b-tetraphenyl-1,3a,3b,4,6a,6b-hexahydro-1,4-digerma-cyclobutadicyclopentene 6-Ethyl-2,6-diphenyl-bicyclo[3.1.0]hexane (1S,2S,4R,5R)-1,2,4,5-Tetraphenyl-tricyclo[3.1.0.02,4]hexane (4R,5S)-4-(3,4-dimethoxyphenyl)-5-nitro-5-(4-nitrobenzyl)tetrahydro-2H-pyran-2-one (1R,2R,3S,4S)-ethyl 1-acetyl-4-hydroxy-3-nitro-2,4-diphenylcyclopentanecarboxylate 3,4-bis-(4-hydroxy-3-methoxy-phenyl)-cyclobutane-1,2-dicarboxylic acid 1r,2c-diacetyl-3t,4t-diphenyl-cyclobutane 3,7-Diphenyl-tetracyclo<3.3.0.02,8.03,7>octan 3,3-Dimethyl-1-phenyl-tricyclo[4.1.0.02,7]heptane (3S,4R)-ethyl 1,2,3,4-tetrahydro-1-methyl-2-oxo-4-p-tolylpyridine-3-carboxylate (2R,3R)-2,3-diphenylcyclopropane-1,1-dimethanol methyl 1-formyloxy-9,9-bis(4-methoxyphenyl)pentacyclo<4.3.0.02,5.03,8.04,7>nonane-4-carboxylate (3-Cyanomethyl-2,4-diphenyl-cyclobutyl)-acetonitrile γ-Truxinsaeure (1R,6S)-1,7-Diphenyl-bicyclo[4.1.0]heptane 4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoic acid 2,5,6-trimethyl-3,4-diphenyl-cyclohex-3-enecarboxylic acid 5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.13,17.18,12.04,7.013,16.019,22>tetracosa-1,3(23),8,10,12(24),17-hexaen (3S,4R)-3,4-diphenyltetracyclo[11.5.0.02,5.06,12]octadeca-1,5,7,10,12,14,17-heptaene (Z)-1,2-bis(trans-2,trans-3-diphenylcyclopropyl)ethene Ethyl 4-(7-phenyl-7-bicyclo[2.2.1]heptanyl)benzoate 5-Methyl-5,6-diphenylcyclohexa-1,3-diene 4,4',4'',4'''-cyclobutane-1,2,3,4-tetrayl-tetrakis-benzamidine (1R,2R,3S,4S)-3,4-Diphenyl-cyclobutane-1,2-dicarboxylic acid bis-dimethylamide 3,4,12,13-Tetraphenylpentacyclo<13.3.1.16,10.02,5.011,14>eicosa-1(19),6,8,10(20),15,17-hexaen 1'-[(tert-butoxy)carbonyl]-4,10-dimethyl-14,33-dinitrospiro(2,12-dioxa-18,22,25,29-tetraazahexacyclo-[29.2.2.23,6.28,11.213,16.222,25]tritetraconta-3,5,8,10,13,15,31,33,34,38,40,42-dodecaene-7,4'-piperidine)-17,30-dione 4,4'-Dibrom-β-truxinsaeure-dimethylester 1ξ-bromo-2r,3c-bis-bromomethyl-1ξ,4t-diphenyl-cyclobutane (Z)-1,2-bis(trans-2,trans-3-diphenylcyclopropyl)ethene Methyl-[3,4,4-triphenyl-thietan-(2Z)-ylidene]-amine