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methyl (E,4R,5R)-4-mesyloxy-5-(tert-butyldimethyl)siloxy-2-hexenoate | 104778-66-7

中文名称
——
中文别名
——
英文名称
methyl (E,4R,5R)-4-mesyloxy-5-(tert-butyldimethyl)siloxy-2-hexenoate
英文别名
methyl (4R,5R,2E)-5-tert-butyldimethylsilyloxy-4-methanesulfonyloxyhexenoate;(2E,4R,5R)-5-(Tert-Butyldimethylsilyloxy)-4-methylsulfonyloxy-2-hexenoic acid methyl ester;methyl (E,4R,5R)-5-[tert-butyl(dimethyl)silyl]oxy-4-methylsulfonyloxyhex-2-enoate
methyl (E,4R,5R)-4-mesyloxy-5-(tert-butyldimethyl)siloxy-2-hexenoate化学式
CAS
104778-66-7
化学式
C14H28O6SSi
mdl
——
分子量
352.524
InChiKey
NQNBCLLWYZUIIQ-CZHKVUGUSA-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):
    2.47
  • 重原子数:
    22
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    87.3
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

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文献信息

  • Synthesis and absolute configuration of lactone II isolated from Streptomyces sp. Go 40/10
    作者:Toshihiko Ueki、Yoshiki Morimoto、Takamasa Kinoshita
    DOI:10.1039/b104920h
    日期:——
    All four possible stereoisomers of lactone II isolated from Streptomyces sp. Go 40/10, an autoregulator, have been efficiently synthesized in a stereoselective manner starting from (S)-malic acid and sorbic acid, and the absolute configuration was determined to be 2S, 3S, 9R, 10S.
    以(S)-苹果酸山梨酸为起始原料,以立体选择性方式高效合成了从自律调节链霉菌 Go 40/10 分离得到的内酯 II 的所有四种可能的立体异构体,并确定其绝对构型为 2S、3S、9R、10S。
  • A simple synthesis of Ω[(E)CHCH]gly dipeptide isosteres via reductive elimination of γ-oxygenated α,β-enoates with alkenylcopper reagents
    作者:Nobutaka Fujiia、Hiromu Habashita、Noriko Shigemori、Akira Otaka、Toshiro Ibuka、Miwa Tanaka、Yoshinori Yamamoto
    DOI:10.1016/s0040-4039(00)93510-x
    日期:1991.9
    Readily available protected forms of δ-amino-γ-msyloxy-α,β-enoates can be converted to protected dipeptide isosteres, Ω[(E)CHCH]Gly, in high yields by reduction with alkenylcopper reagents.
    可以通过烯基试剂还原以高收率将δ-基-γ-甲基氧基-α,β-烯酸酯的现成可用的受保护形式转化为受保护的二肽等排体Ω[(E)CH = CH] Gly。
  • Very high chemoselective, regioselective, and E-stereoselective 1,3-chirality transfer involving reaction of acyclic (E)- and (Z)-.gamma.-mesyloxy .alpha.,.beta.-enoates and organocyanocopper-trifluoroborane reagents. Efficient synthetic routes to functionalized chiral .alpha.-alkyl (E)-.beta.,.gamma.-enoates and (E)-allylic alcohols with high optical purity
    作者:Toshiro Ibuka、Miwa Tanaka、Shinji Nishii、Yoshinori Yamamoto
    DOI:10.1021/ja00195a045
    日期:1989.6
  • Remarkable difference in reactivity of ordinary vinylcopper reagents and vinylzinc halide containing a copper salt towards γ-mesyloxy-α, β-enoates. Synthesis of homochiral 1,4-dienes
    作者:Toshiro Ibuka、Kazuo Nakai、Hiromu Habashita、Kiyoshi Bessho、Nobutaka Fujii、Yukiyasu Chounan、Yoshinori Yamamoto
    DOI:10.1016/s0040-4020(01)80217-9
    日期:——
    Whereas the reaction of gamma-mesyloxy alpha,beta-enoates with vinyl-Cu(CN)M or (vinyl)2Cu(CN)M2 (M = Li or MgX) yielded a reduction product with an (E)-double bond at the beta,gamma-position, treatment of the same substrates with ''higher order'' zinc cuprate reagents or vinyl-ZnCl by the addition of catalytic amount of Cu(I) or Cu(II) salt afforded alpha- and gamma-vinylation products. Both vinylation products were stable 1,4-diene derivatives that are only more difficulty accessed by more traditional means.
  • IBUKA TOSHIRO; NAKAO TOMIO; NISHII SHINJI; YAMAMOTO YOSHINORI, J. AMER. CHEM. SOC., 108,(1986) N 23, 7420-7422
    作者:IBUKA TOSHIRO、 NAKAO TOMIO、 NISHII SHINJI、 YAMAMOTO YOSHINORI
    DOI:——
    日期:——
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