Crystal structure of 7,8,15,16,17-pentathiadispiro[5.2.59.36]heptadecane
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Andreas Link | Carola Schulzke | A. Link | C. Schulzke | Robert Hofstetter | Felix Potlitz | Benedict J Elvers | R. Hofstetter | F. Potlitz | B. J. Elvers
[1] H. Palmstierna,et al. Reactions between Ketones and Ammonium Polysulphide. , 1959 .
[2] A. Papapetropoulos,et al. International Union of Basic and Clinical Pharmacology. CII: Pharmacological Modulation of H2S Levels: H2S Donors and H2S Biosynthesis Inhibitors , 2017, Pharmacological Reviews.
[3] Emma K Davison,et al. Natural Products with Heteroatom-Rich Ring Systems. , 2017, Journal of natural products.
[4] A. Senning,et al. Highly sulfurated heterocycles via dithiiranes and trithietanes as key intermediates. , 2002, The Journal of organic chemistry.
[5] H. Matsunami,et al. The role of metals in mammalian olfaction of low molecular weight organosulfur compounds. , 2017, Natural product reports.
[6] Dejian Huang,et al. Cyclic polysulphide 1,2,4-trithiolane from stinky bean (Parkia speciosa seeds) is a slow releasing hydrogen sulphide (H2S) donor , 2017 .
[7] Robin Taylor,et al. Mercury: visualization and analysis of crystal structures , 2006 .
[8] Jie Cheng,et al. Meat flavor generation from different composition patterns of initial Maillard stage intermediates formed in heated cysteine-xylose-glycine reaction systems. , 2019, Food chemistry.
[9] Pekka Pyykkö,et al. Molecular single-bond covalent radii for elements 1-118. , 2009, Chemistry.
[10] G. Sheldrick. A short history of SHELX. , 2008, Acta crystallographica. Section A, Foundations of crystallography.