(1S,2R,3R,4S)-3,6-dibromocyclohex-5-ene-1,2,4-triol | 1025938-68-4

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (1S,2R,3R,4S)-3,6-dibromocyclohex-5-ene-1,2,4-triol
• CAS: 1025938-68-4
• 化学式: C₆H₈Br₂O₃
• 分子量: 287.936
• InChiKey: RNRQWTIKPHYVFT-KCDKBNATSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.2
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  60.7
• 氢给体数：
  3
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1S,2R,3R,4S)-3,6-dibromocyclohex-5-ene-1,2,4-triol 在 sodium hydride 、 对甲苯磺酸 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 12.5h， 生成
  参考文献：
  名称：

  Chemoenzymatic Total Syntheses of Ribisins A, B, and D, Polyoxygenated Benzofuran Derivatives Displaying NGF-Potentiating Properties

  摘要：

  Total syntheses of the structures, 1, 2, and 4, assigned to the biologically active natural products ribisins A, B, and D, respectively, have been achieved using the microbially derived and enantiomerically pure cis-1,2-dihydrocatechol 5 as starting material. Key steps include Suzuki-Miyaura cross-coupling, intramolecular Mitsunobu, and tandem epoxidation/rearrangement reactions. As a result of these studies, the structures of ribisins A and D have been confirmed while that of congener B was shown to be represented by 31 rather than 2.

  DOI：

  10.1021/jo500210k
• 作为产物：
  描述：

  (1S-顺式)-3-溴-3,5-环己二烯-1,2-二醇 在 N-溴代丁二酰亚胺(NBS) 、 水 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 以77%的产率得到(1S,2R,3R,4S)-3,6-dibromocyclohex-5-ene-1,2,4-triol
  参考文献：
  名称：

  结构和立体化学形式的C 7 N氨基环醇衍生物的酶衍生和同手性顺式-1，2-二氢邻苯二酚的合成。

  摘要：

  的结构和立体异构变化Ç 7 Ñ氨基环醇衍生物2 - 4已被制备，其中使用一种通用和协议的灵活范围，从顺式-1,2- dihydrocatechols 5和6从的全细胞生物转化得到，纯手性代谢物相应的卤代苯。还已经建立了能够合成这些衍生物的对映体形式的反应序列。

  DOI：

  10.1021/acs.orglett.8b03149

文献信息

• Total synthesis and structural revision of an isopanepoxydone analog isolated from <i>Lentinus strigellus</i>
  作者：Yi Man、Shaomin Fu、Juan Chen、Bo Liu

  DOI：10.1039/c8ob01168k

  日期：——

  Asymmetric total synthesis of compound 1, as a proposed molecular structure of a natural product, in 11 steps is described. The inconsistency of the characterization data between our synthesized sample and the natural product prompted us to propose a different molecular structure as compound 2 and accordingly accomplish total synthesis in 9 steps and confirm the structural revision of this natural

  描述了作为天然产物的建议分子结构的化合物1的不对称全合成，共分11个步骤。我们合成的样品与天然产物之间的表征数据不一致，促使我们提出了与化合物2不同的分子结构，并因此完成了9个步骤的全合成，并确认了该天然产物的结构变化。两种总合成均具有高度的区域选择性和非对映选择性的环氧化，Stille交叉偶联和交叉复分解。
• Rapid, Chemoenzymatic Syntheses of the Epoxyquinols ( - )-Bromoxone Acetate and ( - )-Tricholomenyn A
  作者：David M. Pinkerton、Martin G. Banwell、Anthony C. Willis

  DOI：10.1071/ch09469

  日期：——

  The epoxyquinol derivatives (–)-bromoxone acetate (ent-1) and (–)-tricholomenyn A (2) have been prepared from the cis-1,2-dihydrocatechols 3 and 4, respectively. Compounds 3 and 4 are themselves obtained in enantiomerically pure form through the whole-cell biotransformation of the corresponding halobenzene.

  我们分别从顺式-1,2-二氢邻苯二酚 3 和 4 中制备出了环氧喹啉衍生物 (-)-Bromoxone acetate (ent-1) 和 (-)-tricholomenyn A (2)。化合物 3 和 4 是通过相应卤苯的全细胞生物转化以对映体纯形式获得的。
• A Chemoenzymatic Route to the (+)-Form of the Amaryllidaceae Alkaloid Narseronine
  作者：Shuxin Yang、Martin G. Banwell、Anthony C. Willis、Jas S. Ward

  DOI：10.1071/ch14520

  日期：——

  The enzymatically derived and enantiopure cis-1,2-dihydrocatechol 1 has been converted, over 14 one-pot operations, into the (+)-form of the alkaloid narseronine (2). The present study, which complements earlier work that established a route from metabolite 1 to enantiomer (–)-2, involves an N-bromosuccinimide/tri-n-butyltin hydride-mediated cyclisation reaction to construct the unsaturated B-ring lactone of the target compound.

  通过酶法衍生出的对映体纯顺式-1,2-二氢邻苯二酚 1 经过 14 次一锅操作转化为生物碱纳塞龙宁的 (+)- 型 (2)。本研究是对早期工作的补充，早期工作建立了从代谢物 1 到对映体 (-)-2 的路线，涉及 N-溴琥珀酰亚胺/三正丁基锡氢化物介导的环化反应，以构建目标化合物的不饱和 B 环内酯。
• Chemoenzymatic Access to Versatile Epoxyquinol Synthons
  作者：David M. Pinkerton、Martin G. Banwell、Anthony C. Willis

  DOI：10.1021/ol9016657

  日期：2009.10.1

  The enantiomerically pure and readily available metabolites 10-12 have been converted over four simple steps into the epoxyquinol derivatives 22-24, respectively. Compounds 23 and 24 or their immediate precursors have been exploited in efficient total syntheses of (-)-bromoxone (ent-1), (-)-epiepoformin (ent-2), (-)-harveynone (4), (+)-panepophenanthrin (6), and (+)-hexacyclinol (9).
• A Chemoenzymatic Total Synthesis of (+)-Clividine
  作者：Lorenzo V. White、Brett D. Schwartz、Martin G. Banwell、Anthony C. Willis

  DOI：10.1021/jo201005d

  日期：2011.8.5

  The title compound, ent-1, the non-natural enantiomeric form of the lycorenine-type alkaloid (-)-clividine (1), has been prepared using the enantiomerically pure (ee >99.8%) cis-1,2-dihydrocatechol 3 as starting material. A key feature associated with the closing stages of the synthesis involved the diastereoselective addition of a nitrogen-centered radical onto a pendant cyclohexene to establish the cis-fused D-ring and the required stereochemistry at C11b in the final product ent-1.