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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/05/22 18:02:38」(JST)
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English Journal
- Synthesis of novel vitamin D3 analog with an additional ring annulated to A and seco-B rings.
- Sokolowska K1, Sicinski RR2.
- Steroids.Steroids.2014 Sep;87:67-75. doi: 10.1016/j.steroids.2014.05.016. Epub 2014 Jun 10.
- A simple method for the synthesis of yet unknown 5E-vitamin D3 analogs with an additional six-membered ring connecting C-6 and C-19 was developed. Ring-closing metathesis (RCM) was used for efficient formation thereof from the corresponding 5E-isomers of 6-alkenyl vitamin D3 compounds which in turn
- PMID 24928728
- Modular synthesis of bis- and tris-1,2,3-triazoles by permutable sequential azide-aryne and azide-alkyne cycloadditions.
- Yoshida S1, Nonaka T, Morita T, Hosoya T.
- Organic & biomolecular chemistry.Org Biomol Chem.2014 Aug 27. [Epub ahead of print]
- A modular synthetic method for bis- and tris-1,2,3-triazoles that include a benzotriazole structure was developed on the basis of sequential azide-aryne and azide-alkyne cycloadditions. The key to success was efficient halogen-metal exchange reaction-mediated generation of aryne from ortho-iodoaryl
- PMID 25159865
- Concise Stereoselective Synthesis of Oxaspirocycles with 1-Tosyl-1,2,3-triazoles: Application to the Total Syntheses of (±)-Tuberostemospiroline and (±)-Stemona-lactam R.
- Fu J1, Shen H, Chang Y, Li C, Gong J, Yang Z.
- Chemistry (Weinheim an der Bergstrasse, Germany).Chemistry.2014 Aug 21. doi: 10.1002/chem.201403756. [Epub ahead of print]
- A 4-substituted-1-tosyl-1,2,3-triazole-based stereoselective synthesis of structurally diverse oxaspirocycles is reported. The synthesis involves Rh-catalyzed loss of nitrogen from 4-substituted-1-tosyl-1,2,3-triazoles, Grignard reaction, and a ring-closing metathesis reaction as key steps. By emplo
- PMID 25145296
Japanese Journal
- Grignard試薬を用いた不融化石炭ピッチの可溶化と固体及び液体物性解明
- 大学院研究年報 理工学研究科篇 (第45号/2015), 2015-07-01
- NAID 120005675568
- Controlled Polymerization of Electron-deficient Naphthalene-diimide Containing Monomer by Negishi-type Catalyst-transfer Polymerization
- Journal of Photopolymer Science and Technology 28(2), 279-283, 2015
- NAID 130005093858
- Generation of Arynes Using Trimethylsilylmethyl Grignard Reagent for Activation of <i>ortho</i>-Iodoaryl or <i>ortho</i>-Sulfinylaryl Triflates
- Chemistry Letters 44(5), 691-693, 2015
- NAID 130005067968
Related Links
- 基本文献 Grignard, V. Compt. Rend. 1900, 130, 1322. Primitive Review: Shirley, D. A. Org. React. 1954, 8, 28. Huryn, D. M. Comprehensive Organic Synthesis 1991, 1, 49. Recent Progress & Reviews: Franzen, R. G. Tetrahedron 2000 ...
- Grignard Company is your comprehensive resource for specialty chemicals, custom development and private label products, solving complex lubrication, corrosion protection and mold release problems since 1963. ... Grignard ...
Related Pictures
★リンクテーブル★
| リンク元 | 「グリニャール」「グリニヤール」 |
| 拡張検索 | 「Grignard試薬」「Grignard reagent」 |