- Synthesis of Oxindoles by Tandem Heck-Reduction-Cyclization (HRC) from a Single Bifunctional, in Situ Generated Pd/C Catalyst.
[作者:Felpin, Francois-Xavier;Ibarguren, Oier;Nassar-Hardy, Luma;Fouquet, Eric;,期刊:Journal of Organic Chemistry, 页码:1349-1352 , 文章类型: 研究论文,,卷期:2009年74-3]
- A tandem sequence involving palladium-catalyzed sequential Heck-redn.-cyclization transformations in mild conditions has been developed for the synthesis of oxindoles, e.g., I. The protocol involves inexpensive reagents...
- Highly Efficient and Highly Enantioselective Asymmetric Hydrogenation of Ketones with TunePhos/1,2-Diamine-Ruthenium(II) Complexes.
[作者:Li, Wei;Sun, Xianfeng;Zhou, Le;Hou, Guohua;Yu, Shichao;Zhang, Xumu;,期刊:Journal of Organic Chemistry, 页码:1397-1399 , 文章类型: 研究论文,,卷期:2009年74-3]
- The TunePhos/diamine-Ru(II) complex combined with t-BuOK in 2-propanol effectively catalyzes enantioselective hydrogenation of a wide range of simple ketones including arom., heteroarom., a,b-unsatd., and cyclopropyl ket...
- 3,6-Disubstituted carbazole-based bisboronic acids with unusual fluorescence transduction as enantioselective fluorescent chemosensors for tartaric acid.
[作者:Han, Feng;Chi, Lina;Liang, Xiaofen;Ji, Shaomin;Liu, Shasha;Zhou, Fuke;Wu, Yubo;Han, Keli;Zhao, Jianzhang;James, Tony D.;,期刊:Journal of Organic Chemistry, 页码:1333-1336 , 文章类型: 研究论文,,卷期:2009年74-3]
- Carbazole-based bisboronic acids are enantioselective fluorescent sensors for tartaric acid. The fluorescence response toward the enantiomers of tartaric acid at neutral pH displayed enhancement/diminishment. The senso...
- An automatic solid-phase synthesis of peptaibols.
[作者:Hjoerringgaard, Claudia U.;Pedersen, Jan M.;Vosegaard, Thomas;Nielsen, Niels Chr.;Skrydstrup, Troels;,期刊:Journal of Organic Chemistry, 页码:1329-1332 , 文章类型: 研究论文,,卷期:2009年74-3]
- An automated approach to peptaibols using microwave-assisted solid-phase peptide synthesis is demonstrated with a combination of HBTU and acid fluoride mediated couplings for normal and a,a-dialkylated amino acids, resp....
- Quaterthiophenes with Terminal Indeno[1,2-b]thiophene Units as p-Type Organic Semiconductors.
[作者:Pouchain, Laurent;Aleveque, Olivier;Nicolas, Yohann;Oger, Agathe;Le Regent, Charles-Henri;Allain, Magali;Blanchard, Philippe;Roncali, Jean;,期刊:Journal of Organic Chemistry, 页码:1054-1064 , 文章类型: 研究论文,,卷期:2009年74-3]
- Quaterthiophenes 4T, Oct-4T, and Tol-4T based on a central 2,2'-bithiophene core a,w-terminated with 4,4-unsubstituted and 4,4-disubstituted n-octyl or p-tolyl indeno[1,2-b]thiophene were synthesized by Stille or Miyaura...
- Complex Thermal Behavior of 11-cis-Retinal, the Ligand of the Visual Pigments.
[作者:Lopez, Carlos Silva;Alvarez, Rosana;Dominguez, Marta;Nieto Faza, Olalla;de Lera, Angel R.;,期刊:Journal of Organic Chemistry, 页码:1007-1013 , 文章类型: 研究论文,,卷期:2009年74-3]
- Upon heating to 80 癈, 11-cis-retinal yields a mixt. of all-trans-retinal and 13-cis-retinal. This isomerization has been studied by means of d. functional theory methods, and the computational results suggest a close co...
- Practical Ruthenium-Catalyzed Cyclocarbonylation of Allenyl Alcohols in 2,4,6-Collidine Leading to a,b-Unsaturated Lactones: Concise Stereoselective Synthesis of (+)-Isomintlactone.
[作者:Tsubuki, Masayoshi;Takahashi, Kazunori;Honda, Toshio;,期刊:Journal of Organic Chemistry, 页码:1422-1425 , 文章类型: 研究论文,,卷期:2009年74-3]
- We have found that ruthenium-catalyzed cyclocarbonylation of allenyl alcs. in 2,4,6-collidine under atm. pressure of carbon monoxide smoothly proceeds to afford a,b-unsatd. five- and six-membered lactones in moderate to ...
- CuX2-Mediated Halolactonization Reaction of Monoesters of 1,2-Allenyl Phosphonic Acids and Their Suzuki Cross-Coupling Reaction.
[作者:Yu, Fei;Lian, Xiongdong;Zhao, Jinbo;Yu, Yihua;Ma, Shengming;,期刊:Journal of Organic Chemistry, 页码:1130-1134 , 文章类型: 研究论文,,卷期:2009年74-3]
- CuX2-mediated (X = Cl, Br) halolactonization of monoesters of 1,2-allenyl phosphonic acids is presented. The reaction proceeded smoothly under the mild condition for differently substituted allenic substrates giving the...
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