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mp
>350 °C (lit.)
SMILES 字串
CC(C)(C)c1cc2C=[N@@H]3[C@H]4CCCC[C@@H]4[N@H]5=Cc6cc(cc(c6O[Co]35Oc2c(c1)C(C)(C)C)C(C)(C)C)C(C)(C)C
InChI
1S/C36H54N2O2.Co/c1-33(2,3)25-17-23(31(39)27(19-25)35(7,8)9)21-37-29-15-13-14-16-30(29)38-22-24-18-26(34(4,5)6)20-28(32(24)40)36(10,11)12;/h17-22,29-30,39-40H,13-16H2,1-12H3;/q;+2/p-2/b37-21+,38-22+;/t29-,30-;/m0./s1
InChI 密鑰
ZFWPDJKMASHRPT-IKKUFEJKSA-L
應用
用于末端环氧化物的水解动力学拆分和内消旋环氧化物不对称开环的催化剂。
(S,S)-(+)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) may be used as a catalyst for the Jacobsen′s hydrolytic kinetic resolution of racemic epoxides, which is a key step during the multi-step synthesis of (+)-patulolide C, macrosphelides(I and G), (-)-(3S,6R)-3,6-dihydroxy-10-methylundecanoic acid, dodoneine, epidodoneine and protein kinase C epsilon (PKCe) inhibitors.
法律資訊
经 Shasun Chemicals and Drugs Limited 授权销售。
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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A Concise Synthesis of (-)-(3S, 6R)-3, 6-Dihydroxy-10-methylundecanoic Acid Using a Cross-Metathesis Approach.
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Strategies for the modulation of phase II metabolism in a series of PKCe inhibitors.
Bioorganic & Medicinal Chemistry Letters, 24(15), 3398-3402 (2014)
RCM mediated synthesis of macrosphelides I and G.
Tetrahedron Asymmetry, 18(18), 2175-2184 (2007)
Total Synthesis of (+)-Dodoneine and Its 6-Epimer.
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