2-((1R,2R,3R,4R)-2-acetoxy-4-(3-((tert-butyldimethylsilyloxy)methyl)furan-2-yl)-3-(triisopropylsilyloxy)cyclobutyl)ethyl pivalate | 1528747-28-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 2-((1R,2R,3R,4R)-2-acetoxy-4-(3-((tert-butyldimethylsilyloxy)methyl)furan-2-yl)-3-(triisopropylsilyloxy)cyclobutyl)ethyl pivalate
• CAS: 1528747-28-5
• 化学式: C₃₃H₆₀O₇Si₂
• 分子量: 625.006
• InChiKey: JAGSZYKNLYFCRB-RGTFROLJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.99
• 重原子数：
  42.0
• 可旋转键数：
  13.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  84.2
• 氢给体数：
  0.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  2-((1R,2R,3R,4R)-2-acetoxy-4-(3-((tert-butyldimethylsilyloxy)methyl)furan-2-yl)-3-(triisopropylsilyloxy)cyclobutyl)ethyl pivalate 在 potassium carbonate 作用下， 以 甲醇 为溶剂， 反应 3.0h， 以82%的产率得到2-((1R,2R,3R,4R)-2-(3-((tert-butyldimethylsilyloxy)methyl)-furan-2-yl)-4-hydroxy-3-(triisopropylsilyloxy)cyclobutyl)ethyl pivalate
  参考文献：
  名称：

  Studies of the Synthesis of Providencin: Construction and Assembly of Two Major Subunits

  摘要：

  The "northern" sector of the cembranoid diterpene providencin containing a tetrasubstituted cyclobutane was synthesized from the bis(acetonide) of D-glucose using dicyclopentadienylzirconium(0)-mediated oxygen abstraction from a furanose. Oxidative scission of the vinyl substituent of this cyclobutane gave an aldehyde, which was reacted with an alkynylstannane to provide an allenol. Cyclization of the derived allenone with silver nitrate led to a cyclobutylfuran comprising the northern subunit of providencin. The "southern" sector of the cembranoid skeleton containing a trisubstituted iodoalkene attached to an alpha-phenylselenyl-gamma-lactone was synthesized from (R)-glycidol. Negishi carbometalation-iodination established the (E)-iodoalkene, and addition of the lithio dianion of phenylselenoacetic acid to a tosylate generated the substituted lactone. The two sectors were joined via stannylation of the furan of the northern component followed by Stille cross-coupling of the furylstannane with the iodoalkene of the southern subunit. Linkage of the two segments was also made at C12-C13 of providencin using intermolecular aldol condensation of the enolate from the selenyl lactone of the southern portion with an acetaldehyde appendage on the cyclobutane of the northern sector. Closure of the providencin macrocycle from these conjoined subunits was unsuccessful.

  DOI：

  10.1021/jo402485h
• 作为产物：
  描述：

  2-((1R,2R,3R,4S)-2-acetoxy-4-((R)-2-((tert-butyldimethylsilyloxy)methyl)-1-hydroxybuta-2,3-dienyl)-3-(triisopropylsilyloxy)cyclobutyl)ethyl pivalate 在 碳酸氢钠 、 戴斯-马丁氧化剂 作用下， 以 正己烷 、 二氯甲烷 为溶剂， 反应 3.0h， 生成 2-((1R,2R,3R,4R)-2-acetoxy-4-(3-((tert-butyldimethylsilyloxy)methyl)furan-2-yl)-3-(triisopropylsilyloxy)cyclobutyl)ethyl pivalate
  参考文献：
  名称：

  Studies of the Synthesis of Providencin: Construction and Assembly of Two Major Subunits

  摘要：

  The "northern" sector of the cembranoid diterpene providencin containing a tetrasubstituted cyclobutane was synthesized from the bis(acetonide) of D-glucose using dicyclopentadienylzirconium(0)-mediated oxygen abstraction from a furanose. Oxidative scission of the vinyl substituent of this cyclobutane gave an aldehyde, which was reacted with an alkynylstannane to provide an allenol. Cyclization of the derived allenone with silver nitrate led to a cyclobutylfuran comprising the northern subunit of providencin. The "southern" sector of the cembranoid skeleton containing a trisubstituted iodoalkene attached to an alpha-phenylselenyl-gamma-lactone was synthesized from (R)-glycidol. Negishi carbometalation-iodination established the (E)-iodoalkene, and addition of the lithio dianion of phenylselenoacetic acid to a tosylate generated the substituted lactone. The two sectors were joined via stannylation of the furan of the northern component followed by Stille cross-coupling of the furylstannane with the iodoalkene of the southern subunit. Linkage of the two segments was also made at C12-C13 of providencin using intermolecular aldol condensation of the enolate from the selenyl lactone of the southern portion with an acetaldehyde appendage on the cyclobutane of the northern sector. Closure of the providencin macrocycle from these conjoined subunits was unsuccessful.

  DOI：

  10.1021/jo402485h