Organic & Biomolecular Chemistry
基本信息
Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.
CiteScore
| 学科 | 排名 | 百分位 |
|---|---|---|
ChemistryOrganic Chemistry |
36 / 177 | 79% |
期刊统计
投稿信息
投稿网址:
http://mc.manuscriptcentral.com/ob收录体裁:
Full papers
Reviews
Comments
期刊推荐

Biocatalysis and Biotransformation

Chinese Journal of Chemistry

Journal of Chemical Sciences

Electroanalysis

Polycyclic Aromatic Compounds

Journal of the Indian Institute of Science

Topics in Catalysis

Bioorganic & Medicinal Chemistry Letters

Medicinal Chemistry Research

Herald of the Russian Academy of Sciences
相关文献
Support studies toward the hicksoane alkaloids reveal cascade reactions of a (tryptophanamido)methylglycinate
Stephanie Lee, Tilo Söhnel, Jonathan Sperry
DOI: 10.1039/D3OB01596C
Synthesis of the diazatricycloundecane scaffold via gold(i)-catalysed Conia-ene-type 5-exo-dig cyclization and stepwise substituent assembly for the construction of an sp3-rich compound library‡
Tomoya Doi, Kohei Umedera
DOI: 10.1039/D3OB01534C
Electrochemical NaI-mediated one-pot synthesis of guanidines from isothiocyanates via tandem addition-guanylation
Thao Nguyen Thanh Huynh, Khuyen Thu Nguyen, Mongkol Sukwattanasinitt
DOI: 10.1039/D3OB01113E
Adaptive carbonyl umpolung involving a carbanionic carbene Breslow intermediate: an alternative mechanism for NHC-mediated organocatalysis
Rinat R. Aysin
DOI: 10.1039/D3OB01195J
Exploring α-electron-deficiency-induced [1,2]-fluorine migration
Ke Zhang, Xi Chen, Zhoujie Zhang, Caijie Bu, Yong Wu, Jiawei Xu
DOI: 10.1039/D3OB01335A
Umpolung trifluoromethylthiolation of alcohols
Ye Yang, Jiemin Ma, Jiaxiang Zhang, Hu Cai, Wentao Xu
DOI: 10.1039/D3OB01535A
C3-Functionalization of indoles with α-heteroaryl-substituted methyl alcohols
Ethan J. Pazur, Nikhil R. Tasker, Peter Wipf
DOI: 10.1039/D3OB01432K
Base-mediated carboxylation of C-nucleophiles with CO2
Yanlong Luo, Wenbin Huang
DOI: 10.1039/D3OB01367G
Selective and controllable amination and defluoroamidation of α-trifluoromethylstyrene
Shuang-Lian He, Yong-Sheng Bao, Juan Hu, Chaolumen Bai, Dan Liu
DOI: 10.1039/D3OB01595E
Highly asymmetric aldol reaction of isatins and ketones catalyzed by chiral bifunctional primary-amine organocatalyst on water
Xiao-Xiong Lv, Ning Liu, Fei Chen, Hao Zhang, Zhi-Hong Du, Pei Wang, Meng Yuan, Chao Shan Da
DOI: 10.1039/D3OB01227A
您可能还喜欢
4-[4-三氟甲基苯基]恶唑(CAS号:1126636-40-5)通常如何合成?
4-[4-三氟甲基苯基]恶唑通常通过将4-三氟甲基苯酚与异硫氰酸苯酯在有机溶剂中进行酯化反应合成。该反应可在无水条件下,使用适当的催化剂,如四丁基氢氧化铵,以提...
RockPhos Pd G3(CAS号:2009020-38-4)通常如何合成?
RockPhos Pd G3 通常通过钯催化偶联反应合成,使用配体 (2'-Amino-2-biphenylyl)(methanesulfonato-kappa...
1-哌啶甲酰胺(CAS号:2158-03-4)的市场或研究趋势如何?
1-哌啶甲酰胺作为有机合成中的重要中间体,其市场需求主要受医药、农药、染料等行业推动。近年来,随着新药开发和绿色化学的发展,该化合物的研究趋势集中在开发更高效、...
2-(二苯基膦基)乙胺(CAS号:4848-43-5)适用哪些法规指南?
2-(二苯基膦基)乙胺适用于多种法规指南,包括但不限于《全球化学品统一分类和标签制度》(GHS),欧盟《化学品注册、评估、授权和限制》法规(REACH),以及美...
如何储存间苯二甲酸二烯丙酯(CAS号:1087-21-4)?
间苯二甲酸二烯丙酯应储存在阴凉、干燥、通风良好的地方,远离火源和热源。储存容器应密封,避免光照和高温。储存温度应控制在25℃以下,相对湿度应低于80%。避免与其...
什么是间甲苯异硫代异氰酸酯(CAS号:621-30-7)?
间甲苯异硫代异氰酸酯是一种有机化合物,分子式为C7H7NO2S,具有刺激性气味。它是一种重要的有机合成中间体,在合成其他化合物时广泛应用。
在合成中是否有N-Boc-D-苯丙氨醇(CAS号:106454-69-7)的替代品?
在合成中,可以考虑使用N-Cbz-D-苯丙氨醇或N-Fmoc-D-苯丙氨醇作为替代品。这些化合物同样具有保护氨基的功能,且在合成过程中表现出良好的反应性能。
3-羟甲基-2-氧异丙基吡啶(CAS号:954240-50-7)的主要用途是什么?
3-羟甲基-2-氧异丙基吡啶主要用于有机合成领域,可以作为合成其他药物、农药或精细化学品的中间体。此外,它还可能在实验室研究中作为特定反应的前体或溶剂。
6-氨基-9-甲基嘌呤(CAS号:700-00-5)应用于哪些行业?
6-氨基-9-甲基嘌呤目前主要应用于医药行业,作为某些药物的中间体。此外,它还可能用于聚合物、传感器和半导体的某些领域,作为功能性单体或掺杂剂。


![1-(Hexopyranosyloxy)-4a,5-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl 3-phenylacrylate structure 1-(Hexopyranosyloxy)-4a,5-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl 3-phenylacrylate structure](https://cnstatic.chemtradehub.com/structs/192/19210-12-9-ecae.webp)




![2-Bromodibenzo[b,d]furan structure 2-Bromodibenzo[b,d]furan structure](https://cnstatic.chemtradehub.com/structs/86-/86-76-0-1814.webp)
