(2S)-2-amino-3-[3-phenylmethoxy-4-[[(2S,3S,4R,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]methyl]phenyl]propanoic acid | 1054643-80-9

• 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: (2S)-2-amino-3-[3-phenylmethoxy-4-[[(2S,3S,4R,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]methyl]phenyl]propanoic acid
• CAS: 1054643-80-9
• 化学式: C₅₁H₅₃NO₈
• 分子量: 807.984
• InChiKey: INZGDSGZKIHPRR-CJEXUNEQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  60
• 可旋转键数：
  21
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  119
• 氢给体数：
  2
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  乙酸酐 、 (2S)-2-amino-3-[3-phenylmethoxy-4-[[(2S,3S,4R,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]methyl]phenyl]propanoic acid 在 氢氧化钾 作用下， 反应 24.0h， 生成 N-acetyl-3-benzyloxy-4-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranos-1-ylmethyl)-L-phenylalanine
  参考文献：
  名称：

  A Novel General Route for the Synthesis of C-Glycosyl Tyrosine Analogues

  摘要：

  A general method for the synthesis of C-glycosyl amino acids is described here. The stereoisomerically pure tyrosine analigues alpha-L-4 and beta-L-6 are prepared in reasonable overall yields from all l derivatives 10 and 11. The key step is a benzannulation procedure which is employed in the creation of the aromatic ring that bears the amino acid function.

  DOI：

  10.1002/1521-3765(20020415)8:8<1872::aid-chem1872>3.0.co;2-a
• 作为产物：
  描述：

  (2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-ethanal 在 manganese(IV) oxide 、 sodium hydroxide 、 N-溴代丁二酰亚胺(NBS) 、 lithium aluminium tetrahydride 、 氯甲酸乙酯 、 sodium hydride 、 二异丁基氢化铝 、 potassium carbonate 、 三乙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 丙酮 、 甲苯 为溶剂， 反应 78.83h， 生成 (2S)-2-amino-3-[3-phenylmethoxy-4-[[(2S,3S,4R,5R,6R)-3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl]methyl]phenyl]propanoic acid
  参考文献：
  名称：

  A Novel General Route for the Synthesis of C-Glycosyl Tyrosine Analogues

  摘要：

  A general method for the synthesis of C-glycosyl amino acids is described here. The stereoisomerically pure tyrosine analigues alpha-L-4 and beta-L-6 are prepared in reasonable overall yields from all l derivatives 10 and 11. The key step is a benzannulation procedure which is employed in the creation of the aromatic ring that bears the amino acid function.

  DOI：

  10.1002/1521-3765(20020415)8:8<1872::aid-chem1872>3.0.co;2-a

文献信息

• A Novel General Route for the Synthesis of C-Glycosyl Tyrosine Analogues
  作者：Elisabetta Brenna、Claudio Fuganti、Piero Grasselli、Stefano Serra、Sabrina Zambotti

  DOI：10.1002/1521-3765(20020415)8:8<1872::aid-chem1872>3.0.co;2-a

  日期：2002.4.15

  A general method for the synthesis of C-glycosyl amino acids is described here. The stereoisomerically pure tyrosine analigues alpha-L-4 and beta-L-6 are prepared in reasonable overall yields from all l derivatives 10 and 11. The key step is a benzannulation procedure which is employed in the creation of the aromatic ring that bears the amino acid function.