|
- 品牌：DUMABIO
- 产地：上海
- 型号：1mg
- 货号：电询
- 发布日期： 2024-02-27
- 更新日期： 2024-10-09
| 产地 | 上海 |
| 保存条件 | 密封于-20oC阴凉干燥环境。 |
| 品牌 | DUMABIO |
| 货号 | 电询 |
| 用途 | 科研与实验 |
| 检测方法 | 电询 |
| 保质期 | 2年 |
| 适应物种 | 电询 |
| 检测限 | 电询 |
| 数量 | 1000 |
| 包装规格 | 1mg |
| 标记物 | 无 |
| 样本 | 电询 |
| 应用 | 科研试剂 |
| 是否进口 | 否 |
消息：STAB97%@2024技术文献价格已更新
消息：STAB97%@2024技术文献价格已更新
别名:三乙酰氧基硼氢化钠
线性分子式:(CH3COO)3BHNa
CAS号:56553-60-7
分子量:211.94
Beilstein:4047608
MDL编号:MFCD00012211
PubChem化学物质编号:24859012
NACRES:NA.22
检测方案
97%
reaction suitability
reagent type: reductant
mp
116-120 °C (dec.) (lit.)
SMILES string
[Na+].CC(=O)O[BH-](OC(C)=O)OC(C)=O
InChI
1S/C6H10BO6.Na/c1-4(8)11-7(12-5(2)9)13-6(3)10;/h7H,1-3H3;/q-1;+1
InChI key
HHYFEYBWNZJVFQ-UHFFFAOYSA-N
消息：STAB97%@2024技术文献价格已更新
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
-
-
-
说明说明
一般描述
Sodium triacetoxyborohydride (NaBH(OAc)3) is particularly effective in reductive aminations due to its large scope, mildness, and selectivity.[1] It is preferred to sodium cyanoborohydride(NaBH3CN) in many applications due to reduced toxicity of the side products formed, and better yields and reproducibility during synthesis.
应用
三乙酰氧基硼氢化钠[NaBH(OAc)3]可用作以下用途试剂：
酮和醛的还原胺化。[2][3]
与4-氧代戊酸甲酯和苄胺反应，通过还原胺化/内酰胺化制备N-苄基-γ-戊内酰胺。[3]
将亚胺和烯胺还原成相应的胺。[2]
将喹啉和异喹啉还原为相应的四氢衍生物。[2]
烯烃的硼氢化。[4]
合成氮氧双自由基，形成与树枝状大分子连接的高弛豫性末端基团。
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