(δR,2R,5S,6S)-δ,5-Dimethyl-6-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>tetrahydro-2-pyranylbutanol | 152033-09-5

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: (δR,2R,5S,6S)-δ,5-Dimethyl-6-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>tetrahydro-2-pyranylbutanol
• 英文别名: (4R)-4-[(2R,5S,6S)-6-[[tert-butyl(diphenyl)silyl]oxymethyl]-5-methyloxan-2-yl]pentan-1-ol
• CAS: 152033-09-5
• 化学式: C₂₈H₄₂O₃Si
• 分子量: 454.725
• InChiKey: MTEQBAQQQZFDEN-QGNCETNGSA-N

物化性质

• 沸点：
  515.5±36.0 °C(Predicted)
• 密度：
  1.03±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.16
• 重原子数：
  32
• 可旋转键数：
  10
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (δR,2R,5S,6S)-δ,5-Dimethyl-6-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>tetrahydro-2-pyranylbutanol 在 bis(acetylacetonate)oxovanadium 、 palladium dichloride 吡啶 、 2,6-二甲基吡啶 、 叔丁基过氧化氢 、 4-二甲氨基吡啶 、 重铬酸吡啶 、 正丁基锂 、 samarium diiodide 、 草酰氯 、 三甲基溴硅烷 、 3 A molecular sieve 、 4 A molecular sieve 、 氢氟酸 、 四丁基氟化铵 、 水 、 氧气 、 三乙基硅基三氟甲磺酸酯 、 四氯化钛 、 sodium hydride 、 三乙基硼氢化锂 、 potassium carbonate 、 戴斯-马丁氧化剂 、 二甲基亚砜 、 三乙胺 、 三苯基膦 、 copper(l) chloride 、 lithium bromide 、 锌 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 甲醇 、 乙醚 、 乙醇 、 正己烷 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 甲苯 、 乙腈 、 苯 为溶剂， 反应 132.58h， 生成 互变霉素
  参考文献：
  名称：

  Total Synthesis of Tautomycin

  摘要：

  A convergent stereocontrolled synthesis of the antifungal antibiotic tautomycin, a potent protein phosphatases inhibitor, has been achieved first via key aldol coupling of two large subunits, a right-hand C-1-C-21 ketone and a left-hand aldehyde (left from C-22). The C-1-C-10 segment was synthesized through a remote stereochemical control process using a spiroketal template. After joining with the C-11-C-18 segment, the spiroketal moiety was selectively constructed. Then the right-hand C-1-C-21 ketone was synthesized via Roush asymmetric crotylboration. The left-hand aldehyde was prepared from a C-21-C-26 Segment and a dialkylmaleic anhydride segment. Completely stereoselective assemblage of the two subunits, the right-hand and the left-hand, was achieved by employing the Mukaiyama aldol reaction. Further functional group manipulations including desilylation, oxidation at C-2, and deprotection of tert-butyl ester with concomitant anhydride formation provided tautomycin which was identical with the natural product. As a preliminary study, derivatizations and degradation of the natural product were also examined to support the total synthesis.

  DOI：

  10.1021/jo00121a026
• 作为产物：
  描述：

  (tert-butyldiphenylsilanyloxy)acetaldehyde 在 sodium hydroxide 、 9-borabicyclo[3.3.1]nonane dimer 、 正丁基锂 、 三甲基溴硅烷 、 三丁基膦 、 Raney Ni (W-2) 、 双氧水 、 四氯化锡 、 溶剂黄146 、 N,N-二异丙基乙胺 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 吡啶 、 乙醇 、 二氯甲烷 、 水 为溶剂， 生成 (δR,2R,5S,6S)-δ,5-Dimethyl-6-<<<(1,1-dimethylethyl)diphenylsilyl>oxy>methyl>tetrahydro-2-pyranylbutanol
  参考文献：
  名称：

  Synthetic study on tautomycin. Stereocontrolled synthesis of C(1)C(18) fragment using a strategy of selective reduction of spiroketal

  摘要：

  A stereocontrolled synthesis of C(1)-C(18) fragment of tautomycin is accomplished employing asymmetric crotylboration, selective reduction of spiroketal, and addition of crotylstannane as the key steps.

  DOI：

  10.1016/s0040-4039(00)74091-3

文献信息

• Total Synthesis of Tautomycin
  作者：Masato Oikawa、Tohru Ueno、Hideaki Oikawa、Akitami Ichihara

  DOI：10.1021/jo00121a026

  日期：1995.8

  A convergent stereocontrolled synthesis of the antifungal antibiotic tautomycin, a potent protein phosphatases inhibitor, has been achieved first via key aldol coupling of two large subunits, a right-hand C-1-C-21 ketone and a left-hand aldehyde (left from C-22). The C-1-C-10 segment was synthesized through a remote stereochemical control process using a spiroketal template. After joining with the C-11-C-18 segment, the spiroketal moiety was selectively constructed. Then the right-hand C-1-C-21 ketone was synthesized via Roush asymmetric crotylboration. The left-hand aldehyde was prepared from a C-21-C-26 Segment and a dialkylmaleic anhydride segment. Completely stereoselective assemblage of the two subunits, the right-hand and the left-hand, was achieved by employing the Mukaiyama aldol reaction. Further functional group manipulations including desilylation, oxidation at C-2, and deprotection of tert-butyl ester with concomitant anhydride formation provided tautomycin which was identical with the natural product. As a preliminary study, derivatizations and degradation of the natural product were also examined to support the total synthesis.
• Synthetic study on tautomycin. Stereocontrolled synthesis of C(1)C(18) fragment using a strategy of selective reduction of spiroketal
  作者：Masato Oikawa、Hideaki Oikawa、Akitami Ichihara

  DOI：10.1016/s0040-4039(00)74091-3

  日期：1993.7

  A stereocontrolled synthesis of C(1)-C(18) fragment of tautomycin is accomplished employing asymmetric crotylboration, selective reduction of spiroketal, and addition of crotylstannane as the key steps.