(5R,6R)-2-methoxy-5-tert-butyldimethylsilyloxy-6-tert-butyldimethylsilyloxymethyl-1,2-didehydropiperidine | 216860-73-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: (5R,6R)-2-methoxy-5-tert-butyldimethylsilyloxy-6-tert-butyldimethylsilyloxymethyl-1,2-didehydropiperidine
• 英文别名: tert-butyl-[[(2R,3R)-3-[tert-butyl(dimethyl)silyl]oxy-6-methoxy-2,3,4,5-tetrahydropyridin-2-yl]methoxy]-dimethylsilane
• CAS: 216860-73-0
• 化学式: C₁₉H₄₁NO₃Si₂
• 分子量: 387.71
• InChiKey: JWAIIQXUNBVJBC-HZPDHXFCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.61
• 重原子数：
  25
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.95
• 拓扑面积：
  40
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (5R,6R)-2-methoxy-5-tert-butyldimethylsilyloxy-6-tert-butyldimethylsilyloxymethyl-1,2-didehydropiperidine 在 bis(acetylacetonate)nickel(II) 、 platinum on activated charcoal lithium hydroxide 、 正丁基锂 、 四丁基氟化铵 、 氢气 、 二异丙胺 、 N,N-二异丙基乙胺 、 2-氯-1-甲基吡啶鎓三氟甲烷磺酸盐 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 正己烷 、 氯仿 、 水 、 乙酸乙酯 、 乙腈 为溶剂， -78.0~70.0 ℃ 、344.74 kPa 条件下， 反应 126.75h， 生成 (2R,3R,6R,7R)-7-ethyl-3-hydroxy-2-hydroxymethyl-8-oxo-1-azabicyclo[4.2.0]octane
  参考文献：
  名称：

  Synthesis of Carbacephems from Serine

  摘要：

  Carbacephems have been synthesized from D-serine by two routes involving construction first of the six-membered ring followed by cyclization to give the bicyclic beta-lactam. In one route, alkylation of a lactim ether was accomplished with Ni(Acac)(2) as a catalyst. The desired R stereochemistry at the carbon corresponding to C-6 of the cephem was obtained by stereospecific hydrogenation of a vinylogous carbamate. The second route involved a stereospecific Michael cyclization to give the same C-6 stereochemistry. Closure of a piperidyl beta-amino acid intermediate common to both routes was accomplished using a modified Mukaiyama reagent found to be superior in our system to the traditional reagent. The resulting carbacephem core was stereospecifically substituted at C-7 with an ethyl or amino functionality. The ethylated intermediate was transformed into a stable enol triflate useful for the further elaboration of biologically important carbacephems.

  DOI：

  10.1021/jo980592s
• 作为产物：
  描述：

  (4R,5R)-4-Allyl-2,2-dimethyl-5-<(phenylsulfonyl)amino>-1,3-dioxane 在 ruthenium trichloride 咪唑 、 盐酸 、 4-二甲氨基吡啶 、 sodium periodate 、 9-borabicyclo[3.3.1]nonane dimer 、 sodium naphthalenide 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 四氢呋喃 、 甲醇 、 四氯化碳 、 乙二醇二甲醚 、 phosphate buffer 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 反应 206.5h， 生成 (5R,6R)-2-methoxy-5-tert-butyldimethylsilyloxy-6-tert-butyldimethylsilyloxymethyl-1,2-didehydropiperidine
  参考文献：
  名称：

  Synthesis of Carbacephems from Serine

  摘要：

  Carbacephems have been synthesized from D-serine by two routes involving construction first of the six-membered ring followed by cyclization to give the bicyclic beta-lactam. In one route, alkylation of a lactim ether was accomplished with Ni(Acac)(2) as a catalyst. The desired R stereochemistry at the carbon corresponding to C-6 of the cephem was obtained by stereospecific hydrogenation of a vinylogous carbamate. The second route involved a stereospecific Michael cyclization to give the same C-6 stereochemistry. Closure of a piperidyl beta-amino acid intermediate common to both routes was accomplished using a modified Mukaiyama reagent found to be superior in our system to the traditional reagent. The resulting carbacephem core was stereospecifically substituted at C-7 with an ethyl or amino functionality. The ethylated intermediate was transformed into a stable enol triflate useful for the further elaboration of biologically important carbacephems.

  DOI：

  10.1021/jo980592s

文献信息

• Synthesis of Carbacephems from Serine
  作者：James J. Folmer、Carles Acero、Dung L. Thai、Henry Rapoport

  DOI：10.1021/jo980592s

  日期：1998.11.1

  Carbacephems have been synthesized from D-serine by two routes involving construction first of the six-membered ring followed by cyclization to give the bicyclic beta-lactam. In one route, alkylation of a lactim ether was accomplished with Ni(Acac)(2) as a catalyst. The desired R stereochemistry at the carbon corresponding to C-6 of the cephem was obtained by stereospecific hydrogenation of a vinylogous carbamate. The second route involved a stereospecific Michael cyclization to give the same C-6 stereochemistry. Closure of a piperidyl beta-amino acid intermediate common to both routes was accomplished using a modified Mukaiyama reagent found to be superior in our system to the traditional reagent. The resulting carbacephem core was stereospecifically substituted at C-7 with an ethyl or amino functionality. The ethylated intermediate was transformed into a stable enol triflate useful for the further elaboration of biologically important carbacephems.