Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Jacobsen epoxidation"'
Publikováno v:
Pharmaceutical Fronts, Vol 03, Iss 03, Pp e113-e118 (2021)
Abstract This study reported an asymmetric synthesis of 1,2-limonene epoxides. The absolute stereochemistry was controlled by a Jacobsen epoxidation of cis-1,2-limonene epoxide (with diastereomeric excess of 98%) and trans-1,2-limonene epoxide (with
Externí odkaz:
https://doaj.org/article/e077b38b0bb142febb61e3030459d19f
Autor:
Mark Lautens, Egor M. Larin
Publikováno v:
Synfacts. 2019:0517
Publikováno v:
Chemistry - A European Journal. 19:4532-4537
A concise and largely catalysis-based approach to the potent algal toxin polycavernoside A (1) is described that intercepts a late-stage intermediate of a previous total synthesis; from there on, this challenging target can be reached in a small numb
Autor:
Kiwan Jang, Gautam Dupati, Li-Juan Meng, B.V.D. Vijaykumar, Zhu-Bo Li, Hua Zuo, Dong-Soo Shin
Publikováno v:
Tetrahedron: Asymmetry. 23:1029-1037
With the aim of discovering new molecules with potassium channel activating properties, we have designed and synthesized derivatives with structural similarity to cromakalim, an important molecule which shows specific affinity toward potassium channe
Autor:
S. S. Mandal, J. S. Yadav
Publikováno v:
Synlett. 2011:2803-2806
The enantioselective synthesis of bioactive butenolides isocladospolide B, cladospolide B, and cladospolide-C has been achieved from (S)-propylene oxide. Of the three stereogenic centers, the C-4/C-5 vic-diol was obtained using diastereo- and enantio
Publikováno v:
Organic Letters. 11:4592-4595
It is proposed that facial selectivity in the Jacobsen epoxidation is determined by electrostatic and steric factors with a two-step pathway involving a carbocationic intermediate.
Autor:
Adrian Hall, Robert Haigh, Michael P. Coogan, Robert Leyshon Jenkins, Nicholas C. O. Tomkinson, C. Jones, Lisa D. Harris, David E. Hibbs
Publikováno v:
Tetrahedron. 59:7389-7395
A new approach to the rational design of Lewis acids based on face-face π-π interactions is described. The synthesis of two novel diols (-)(1R,3R)-2,2-dimethyl-1,2,3,4-tetrahydronaphthalene-1,3-diol (I) and (-)(1S,3R)-trans-2,2-dimethyl-1,2,3,4-tet
Publikováno v:
Reactive and Functional Polymers. 53:103-112
Herein we report preliminary results on enantioselective epoxidations of styrene using molecular imprint polymers incorporating an analog of the Jacobsen epoxidation catalyst. We have synthesized molecular imprint polymers (MIPs) containing the pre-c
Publikováno v:
Organic Letters. 4:3571-3574
[reaction: see text] Two methods have been developed for the synthesis of epoxide 36. The first uses (+)-pulegone 25 as an enantiopure starting material and introduces the requisite intricacy of target 22 in 12 operations. The second method employs a
Autor:
Tien Nguyen
Publikováno v:
C&EN Global Enterprise. 95:9-9
Ketamine is a drug that has been administered as an anesthetic for more than 50 years. A decade ago, scientists found that a small dose of ketamine can also serve as a fast-acting antidepressant. Then last year, researchers discovered that ketamine