(R)-1-naphthalen-1-yl-but-3-en-1-ol

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (R)-1-naphthalen-1-yl-but-3-en-1-ol
• 英文别名: (R)-1-(1-naphthyl)-3-buten-1-ol；1-(naphthalen-1-yl)but-3-en-1-ol；(1R)-1-naphthalen-1-ylbut-3-en-1-ol
• 化学式: C₁₄H₁₄O
• 分子量: 198.265
• InChiKey: FFNKLJQFZFTUHS-CQSZACIVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  1-(α-naphthyl)-3-buten-1-yl acetate 以88%的产率得到
  参考文献：
  名称：

  BASAVAIAH, D.;DHARMA, RAO P., SYNTH. COMMUN. , 20,(1990) N9, C. 2945-2949

  摘要：

  DOI：

文献信息

• Highly Enantioselective Allylation of Arylaldehydes Catalyzed by a Silver(I)-Chiral Binaphthylthiophosphoramide
  作者：Chun-Jiang Wang、Min Shi

  DOI：10.1002/ejoc.200300099

  日期：2003.8

  diphenylthiophosphoramide L2 prepared from diphenylthiophosphinic chloride and ?-(+)-N-ethyl-1,1'-binaphthyl-2,2'-diamine 2 was used as a catalytic chiral ligand in the siver(I)-catalyzed enantioselective allylation reaction of arylaldehydes with allyltribuyltin to furnish high ee (up to 98%) of the homoallylic alcohols.

  由二苯基硫代次膦酰氯和 α-(+)-N-乙基-1,1'-联萘-2,2'-二胺 2 制备的手性二苯基硫代磷酰胺 L2 在银 (I) 催化的对映选择性烯丙基化反应中用作催化手性配体芳基醛与烯丙基三烷基锡的反应可提供高 ee（高达 98%）的高烯丙醇。
• Proline-Based <i>N</i>-Oxides as Readily Available and Modular Chiral Catalysts. Enantioselective Reactions of Allyltrichlorosilane with Aldehydes
  作者：John F. Traverse、Yu Zhao、Amir H. Hoveyda、Marc L. Snapper

  DOI：10.1021/ol050814q

  日期：2005.7.1

  as an effective catalyst for the reaction of allyltrichlorosilane with aryl and alpha,beta-unsaturated aldehydes at room temperature to afford the desired homoallylic alcohols in up to 92% ee. The chiral catalyst can be easily prepared from optically pure proline in three simple steps and 60% overall yield.

  [反应：请参见文字]。鉴定出基于脯氨酸的N-氧化物，其可作为烯丙基三氯硅烷与芳基和α，β-不饱和醛在室温下反应的有效催化剂，以提供高达92％ee的所需均烯丙基醇。可以通过三个简单的步骤由旋光纯的脯氨酸轻松制备手性催化剂，且总收率为60％。
• Synthetically amenable amide derivatives of tosylated-amino acids as organocatalysts for enantioselective allylation of aldehydes: computational rationale for enantioselectivity
  作者：Debashis Ghosh、Debashis Sahu、S. Saravanan、Sayed H. R. Abdi、Bishwajit Ganguly、Noor-ul H. Khan、Rukhsana I. Kureshy、Hari C. Bajaj

  DOI：10.1039/c3ob27513b

  日期：——

  A phenylalanine derived chiral amide is developed that serves as an effective organocatalyst for the reaction of allyltrichlorosilane with aryl, hetero-aryl and α,β-unsaturated aldehydes to afford the desired homoallylic alcohols in good yield (up to 90%) and high enantioselectivity (up to 99%). The experimental results and DFT calculations suggest that para substituted aromatic aldehydes as substrate show higher ee in the product than their ortho/meta counterparts. The 1H and 13C NMR spectra study corroborated the calculated results. The chiral organocatalyst can be easily synthesized from optically pure phenylalanine in two simple steps with 90% overall yield.

  开发了一种由苯丙氨酸衍生的手性酰胺，它作为有效的有机催化剂，用于烯丙基三氯硅烷与芳基、杂芳基和α,β-不饱和醛的反应，以良好的产率（高达90%）和高对映选择性（高达99%）得到所需的同烯丙基醇。实验结果和DFT计算表明，与邻/间位取代的芳香醛相比，对位取代的芳香醛作为底物在产物中显示出更高的对映体过量值。1H和13C NMR光谱学研究证实了计算结果。手性有机催化剂可以通过两个简单步骤从光学纯苯丙氨酸轻松合成，总产率为90%。
• A catalytic enantioselective allylation reaction of aldehydes in an aqueous medium
  作者：Teck-Peng Loh、Jian-Rong Zhou

  DOI：10.1016/s0040-4039(00)00801-7

  日期：2000.7

  A modified Yamamoto–Yanagisawa's catalyst (S)-Tol-BINAP·AgNO3 was successfully applied to a catalytic enantioselective allylation reaction of aldehydes in an aqueous system. The reactions with aromatic aldehydes afforded the desired products in high yields with good stereoselectivities.

  改良的Yamamoto-Yanagisawa催化剂（S）-Tol-BINAP·AgNO 3被成功地用于水体系中醛的催化对映选择性烯丙基化反应。与芳族醛的反应以高收率和良好的立体选择性提供了所需的产物。
• Catalytic enantioselective allylation of aldehydes via a moisture-tolerant chiral BINOL–In(III) complex
  作者：Yong-Chua Teo、Ee-Ling Goh、Teck-Peng Loh

  DOI：10.1016/j.tetlet.2005.07.064

  日期：2005.9

  A moisture-tolerant chiral indium complex has been developed to effect good enantioselectivities in the addition of allyltributylstannanes to aldehydes. The allylation of a variety of aromatic, α,β-unsaturated and aliphatic aldehydes resulted in both moderate to good yields and high enantioselectivities (up to 86% ee).

  已经开发了一种耐湿性手性铟络合物，以在向醛中添加烯丙基三丁基锡烷来实现良好的对映选择性。各种芳香族，α，β-不饱和醛和脂肪族醛的烯丙基化导致中度到良好的收率以及高对映选择性（高达86％ee）。