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- Reactions of terpenoids in strong acids. Part 2. Novel cyclisations of citronellol and the isomers of citral. Derek V. Banthorpe, Paul A. Boullier
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 114
- “Old” chemistry in a new context: photocleavable 2-oxoacetate-containing latex dispersions and core–shell microcapsules for the controlled release of volatile compounds. Marine Charlon, Alain Trachsel, Nicolas Paret, Laurence Frascotti, Damien L. Berthier, Andreas Herrmann
, Polym. Chem.
, 2015
, 6
, 3224
- Indoor partitioning and potential thirdhand exposure to carbonyl flavoring agents added in e-cigarettes and hookah tobacco. Shuang Wu, Erica Kim, Dilini Vethanayagam, Ran Zhao
, Environ. Sci.: Processes Impacts
, 2022
, 24
, 2294
- BINOL-Al catalysed asymmetric cyclization and amplification: preparation of optically active menthol analogs. Hisanori Itoh, Hironori Maeda, Shinya Yamada, Yoji Hori, Takashi Mino, Masami Sakamoto
, Org. Biomol. Chem.
, 2015
, 13
, 5817
- Citral mitigates inflammation of Caco-2 cells induced by Cronobacter sakazakii. Du Guo, Fangting Bai, Xiangjun Zhan, Wenting Zhang, Tong Jin, Yutang Wang, Xiaodong Xia, Chao Shi
, Food Funct.
, 2022
, 13
, 3540
- Supported ionic liquids
catalysts for fine chemicals: citral hydrogenation. Jyri-Pekka Mikkola, Pasi Virtanen, Hannu Karhu, Tapio Salmi, Dmitry Yu. Murzin
, Green Chem.
, 2006
, 8
, 197
- Aerobic epoxidation of β-ionone in water under mild conditions using aldehydes as catalyst precursors. Xu Zhang, Zijie Wei, Lei Yu
, React. Chem. Eng.
, 2023
, 8
, 1700
- Fabrication of core–shell type poly(NIPAm)-encapsulated citral and its application on bamboo as an anti-molding coating. Rui Peng, Chungui Du, Ailian Hu, Qi Li, Jingjing Zhang, Weigang Zhang, Fangli Sun
, RSC Adv.
, 2021
, 11
, 36884
- Highly efficient and practical aerobic oxidation of alcohols by inorganic-ligand supported copper catalysis. Zheyu Wei, Shi Ru, Qixin Zhao, Han Yu, Gang Zhang, Yongge Wei
, Green Chem.
, 2019
, 21
, 4069
- Hydrogenation of citral: a wide-spread model reaction for selective reduction of α,β-unsaturated aldehydes. Achim Stolle, Thomas Gallert, Christine Schmöger, Bernd Ondruschka
, RSC Adv.
, 2013
, 3
, 2112