## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
✦ LIBER ✦
Synthesis of camphorsulfonamide-based quinoline ligands and their N-oxides: first use in the enantioselective addition of organozinc reagents to aldehydes
✍ Scribed by Ricardo Martínez; Luca Zoli; Pier Giorgio Cozzi; Diego J. Ramón; Miguel Yus
- Book ID
- 108284397
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 253 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
ChemInform Abstract: Synthesis of Campho
✍
Ricardo Martinez; Luca Zoli; Pier Giorgio Cozzi; Diego J. Ramon; Miguel Yus
📂
Article
📅
2009
🏛
John Wiley and Sons
⚖ 27 KB
👁 2 views
Synthesis of new Schiff base-camphorsulf
✍
Jiangtao Sun; Xu Pan; Zhenya Dai; Chengjian Zhu
📂
Article
📅
2008
🏛
Elsevier Science
🌐
English
⚖ 202 KB
Synthesis of chiral ligands derived from
✍
Jun Lu; Xuenong Xu; Cunde Wang; Jiangang He; Yuefei Hu; Hongwen Hu
📂
Article
📅
2002
🏛
Elsevier Science
🌐
French
⚖ 131 KB
A novel procedure for selective direct N,N-alkylation of the chiral Betti base was developed, and a new family of chiral ligands, (S)-1-(a-cycloaminobenzyl)-2-naphthols, were prepared. The ligands with five-and six-membered cyclic amines showed highly efficient asymmetric induction in the addition o
Synthesis of Chiral Ligands Derived from
✍
Jun Lu; Xuenong Xu; Cunde Wang; Jiangang He; Yuefei Hu; Hongwen Hu
📂
Article
📅
2003
🏛
John Wiley and Sons
⚖ 120 KB
👁 2 views
ChemInform Abstract: Synthesis of New Sc
✍
Jiangtao Sun; Xu Pan; Zhenya Dai; Chengjian Zhu
📂
Article
📅
2009
🏛
John Wiley and Sons
⚖ 30 KB
👁 2 views
Solid-Phase Synthesis of Chiral N -Acyle
✍
Sprout, Christopher M.; Richmond, Meaghan L.; Seto, Christopher T.
📂
Article
📅
2004
🏛
American Chemical Society
🌐
English
⚖ 133 KB