摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(1S,2S,3R,5S)-(2-氨基-2,6,6-三甲基-双环[3.1.1]庚-3-基)-甲醇 | 327611-65-4

中文名称
(1S,2S,3R,5S)-(2-氨基-2,6,6-三甲基-双环[3.1.1]庚-3-基)-甲醇
中文别名
——
英文名称
(1S,2S,3R,5S)-2-amino-3-hydroxymethyl-2,6,6-trimethylbicyclo[3.1.1]heptane
英文别名
(1S,2S,3R,5S)-2-amino-3-hydroxymethylpinane;(1S,2S,3R,5S)-(2-Amino-2,6,6-trimethyl-bicyclo[3.1.1]hept-3-yl)-methanol;[(1S,2S,3R,5S)-2-amino-2,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]methanol
(1S,2S,3R,5S)-(2-氨基-2,6,6-三甲基-双环[3.1.1]庚-3-基)-甲醇化学式
CAS
327611-65-4
化学式
C11H21NO
mdl
——
分子量
183.294
InChiKey
VETFELSGHLFPFA-UYAYMFIHSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    46.2
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:f96047437bf00d7794e7d736fb785191
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (1S,2S,3R,5S)-(2-氨基-2,6,6-三甲基-双环[3.1.1]庚-3-基)-甲醇碘甲烷 作用下, 以 甲醇甲苯 为溶剂, 反应 10.0h, 生成 (1S,2S,7R,9S)-4-phenylimino-2,10,10-trimethyl-5-oxa-3-azatricyclo[7.1.1.02,7]undecane
    参考文献:
    名称:
    Synthesis and transformations of enantiomeric 1,2-disubstituted monoterpene derivatives
    摘要:
    Regio- and stereospecific addition of chlorosulfonyl isocyanate to (+)- and (-)-alpha -pinene I resulted in enantiomerically pure beta -lactams 2, which were converted to enantiomeric beta -amino esters 3 and 1,3-amino alcohols 4 and 6 with ee >99%. The resulting 1,3-difunctional compounds 3, 4 and 6 were transformed to fused saturated 1,3-heterocycles such as tetrahydro-1,3-oxazines 7 and 9, 2,4-pyrimidinedione 11 and 2-thioxopyrimidin-4-one 13 enantiomers. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(00)00435-3
  • 作为产物:
    描述:
    (+)-α-蒎烯盐酸 、 lithium aluminium tetrahydride 、 potassium hydroxide 、 sodium sulfite 作用下, 以 四氢呋喃 为溶剂, 反应 64.0h, 生成 (1S,2S,3R,5S)-(2-氨基-2,6,6-三甲基-双环[3.1.1]庚-3-基)-甲醇
    参考文献:
    名称:
    α-Pinene-type chiral Schiff bases as tridentate ligands in asymmetric addition reactions
    摘要:
    A group of tridentate Schiff bases derived from (+)-alpha-pinene were synthesized. The steric effects in the transition state, the importance of pi-pi stacking interactions as well as the electronic effects of aryl aldehydes according to Hammett constant values in the enantioselective addition of Et2Zn to aldehydes with the use of Schiff bases as chiral ligands are described. Also, a variety of aldehydes were cyanated using a catalyst prepared in situ from titanium tetraisopropoxide and chiral Schiff bases. The influence of a conjugated double-bond in the cyanation substrates on enantioselectivity was observed. The chemical structures of the chiral Schiff base-titanium alkoxide complexes are discussed based on their H-1 and C-13 NMR spectra. 3D models of the Zn-2-complex catalyst and Ti-complex catalyst containing alpha-pinane-type Schiff bases based on X-ray diffraction experiments are postulated. The models presented were consistent with the reported chirality of the addition product and observed ee. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetasy.2011.03.013
点击查看最新优质反应信息

文献信息

  • Enantioselective addition of diethylzinc to aldehydes catalyzed by γ-amino alcohols derived from (+)- and (−)-α-pinene
    作者:Zsolt Szakonyi、Árpád Balázs、Tamás A. Martinek、Ferenc Fülöp
    DOI:10.1016/j.tetasy.2005.12.011
    日期:2006.1
    Primary, secondary and tertiary γ-amino alcohols 4, 5, 7 and 9 and 1,3-diamine 6 were synthesized from (+)- and ()-α-pinene 1 via chiral N-Boc β-amino ester 3a and carboxamide 3b. The amino alcohols and diamine obtained were applied as chiral catalysts in the enantioselective addition of diethylzinc to aromatic aldehydes, resulting in chiral 1-aryl-1-propanols. The first evidence of the substituent-dependent
    伯,仲和叔γ-基醇4,5,7和9和1,3-二胺6购自(+)合成-和( - ) - α蒎烯1通过手性Ñ -Bocβ基酯3A和羧酰胺3b。所获得的基醇和二胺在将二乙基对映体选择性加成到芳族醛中时用作手性催化剂,得到手性的1-芳基-1-丙醇。观察到1,3-基醇催化剂的取代基依赖性对映选择性的第一个证据,并且该现象是通过从头算平使用分子模型来解释的。
  • New chiral Schiff bases derived from (+)- and (−)-α-pinenes in the metal complex catalyzed asymmetric oxidation of sulfides
    作者:E. A. Koneva、K. P. Volcho、D. V. Korchagina、N. I. Komarova、A. I. Kochnev、N. F. Salakhutdinov、A. G. Tolstikov
    DOI:10.1007/s11172-008-0017-8
    日期:2008.1
    New chiral Schiff bases were derived from (+)- and ()-α-pinenes for the first time. Coordinated to vanadium ions, they can be used as ligands in catalytic oxidation of sulfides into chiral sulfoxides. Conditions for the asymmetric oxidation of thioanisole to methyl phenyl sulfoxide in optical purity up to 32% were found. Variation of substituents in the ligand has a significant effect not only on
    新的手性席夫碱首次由 (+)- 和 (-)-α-蒎烯衍生而来。它们与钒离子配位,可用作将硫化物催化氧化为手性亚砜的配体。发现了将苯醚不对称氧化为光学纯度高达 32% 的甲基苯基亚砜的条件。配体中取代基的变化不仅对反应的对映选择性有显着影响,而且对形成的亚砜的绝对构型也有显着影响。
  • New chiral ligands based on (+)-α-pinene
    作者:E. A. Koneva、D. V. Korchagina、Yu. V. Gatilov、A. M. Genaev、A. P. Krysin、K. P. Volcho、A. G. Tolstikov、N. F. Salakhutdinov
    DOI:10.1134/s1070428010080014
    日期:2010.8
    A number of new chiral ligands were synthesized starting from an accessible monoterpene, (+)-alpha-pinene. The new ligands were used in the vanadium-catalyzed oxidation of sulfides to chiral sufoxides.
  • Synthesis, Antimicrobial Evaluation, and Structure–Activity Relationship of α-Pinene Derivatives
    作者:Preeti Dhar、PuiYee Chan、Daniel T. Cohen、Fadi Khawam、Sarah Gibbons、Teresa Snyder-Leiby、Ellen Dickstein、Prashant Kumar Rai、Geeta Watal
    DOI:10.1021/jf403586t
    日期:2014.4.23
    Several (+)- and (-)-alpha-pinene derivatives were synthesized and evaluated for their antimicrobial activity toward Gram-positive bacteria Micrococcus luteus and Staphylococcus aureus, Gram-negative bacterium Escherichia coli, and the unicellular fungus Candida albicans using bioautographic assays. (+)-alpha-Pinene 1a showed modest activity against the test organisms, whereas (-)-alpha-pinene 1b showed no activity at the tested concentration. Of all the alpha-pinene derivatives evaluated, the beta-lactam derivatives (10a and 10b) were the most antimicrobial. The increase in the antimicrobial activity of 10a compared to la ranged from nearly 3.5-fold (C. albicans) to 43-fold (S. aureus). The mean +/- standard deviation for the zone of inhibition (mm) for 10a (C. albicans) was 31.9 +/- 4.3 and that for S. aureus was 51.1 +/- 2.9. Although (-)-alpha-pinene 1b was not active toward the test microorganisms, the corresponding beta-lactam 10b, amino ester 13b, and amino alcohol 14b showed antimicrobial activity toward the test microorganisms. The increase in the antimicrobial activity of lob compared to 1b ranged from 32-fold (S. aureus) to 73-fold (M. luteus). The mean +/- standard deviation for the zone of inhibition (mm) for 10b (S. aureus) was 32.0 +/- 0.60 and that for M. luteus was 73.2 +/- 0.30.
查看更多

同类化合物

(5β,6α,8α,10α,13α)-6-羟基-15-氧代黄-9(11),16-二烯-18-油酸 (3S,3aR,8aR)-3,8a-二羟基-5-异丙基-3,8-二甲基-2,3,3a,4,5,8a-六氢-1H-天青-6-酮 (2Z)-2-(羟甲基)丁-2-烯酸乙酯 (2S,4aR,6aR,7R,9S,10aS,10bR)-甲基9-(苯甲酰氧基)-2-(呋喃-3-基)-十二烷基-6a,10b-二甲基-4,10-dioxo-1H-苯并[f]异亚甲基-7-羧酸盐 (1aR,4E,7aS,8R,10aS,10bS)-8-[((二甲基氨基)甲基]-2,3,6,7,7a,8,10a,10b-八氢-1a,5-二甲基-氧杂壬酸[9,10]环癸[1,2-b]呋喃-9(1aH)-酮 (+)顺式,反式-脱落酸-d6 龙舌兰皂苷乙酯 龙脑香醇酮 龙脑烯醛 龙脑7-O-[Β-D-呋喃芹菜糖基-(1→6)]-Β-D-吡喃葡萄糖苷 龙牙楤木皂甙VII 龙吉甙元 齿孔醇 齐墩果醛 齐墩果酸苄酯 齐墩果酸甲酯 齐墩果酸溴乙酯 齐墩果酸二甲胺基乙酯 齐墩果酸乙酯 齐墩果酸3-O-alpha-L-吡喃鼠李糖基(1-3)-beta-D-吡喃木糖基(1-3)-alpha-L-吡喃鼠李糖基(1-2)-alpha-L-阿拉伯糖吡喃糖苷 齐墩果酸 beta-D-葡萄糖酯 齐墩果酸 beta-D-吡喃葡萄糖基酯 齐墩果酸 3-乙酸酯 齐墩果酸 3-O-beta-D-葡吡喃糖基 (1→2)-alpha-L-吡喃阿拉伯糖苷 齐墩果酸 齐墩果-12-烯-3b,6b-二醇 齐墩果-12-烯-3,24-二醇 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,11-二酮 齐墩果-12-烯-2α,3β,28-三醇 齐墩果-12-烯-29-酸,3,22-二羟基-11-羰基-,g-内酯,(3b,20b,22b)- 齐墩果-12-烯-28-酸,3-[(6-脱氧-4-O-b-D-吡喃木糖基-a-L-吡喃鼠李糖基)氧代]-,(3b)-(9CI) 齐墩果-12-烯-28-酸,3,7-二羰基-(9CI) 齐墩果-12-烯-28-酸,3,21,29-三羟基-,g-内酯,(3b,20b,21b)-(9CI) 鼠特灵 鼠尾草酸醌 鼠尾草酸 鼠尾草酚酮 鼠尾草苦内脂 黑蚁素 黑蔓醇酯B 黑蔓醇酯A 黑蔓酮酯D 黑海常春藤皂苷A1 黑檀醇 黑果茜草萜 B 黑五味子酸 黏黴酮 黏帚霉酸