𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Chiral C2-Symmetric 2,5-Disubstituted Pyrrolidine Derivatives as Catalytic Chiral Ligands in the Reactions of Diethylzinc with Aryl Aldehydes.

✍ Scribed by M. SHI; Y. SATOH; Y. MASAKI


Publisher
John Wiley and Sons
Year
2010
Weight
39 KB
Volume
29
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis


1998 stereochemistry stereochemistry (general, optical resolution) O 0030 50 -037 Chiral C 2 -Symmetric 2,5-Disubstituted Pyrrolidine Derivatives as Catalytic Chiral Ligands in the Reactions of Diethylzinc with Aryl Aldehydes.

-The scope of the title compounds as chiral catalysts in the asymmetric addition of diethylzinc to aryl aldehydes is investigated. An explanation for the unexpected inversion of enantioselectivity observed in the preparation of (S)-(IIIf,g) is not given. -(SHI, M.;


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Chiral C2-Symmetric
✍ Min Shi; Jian-Kang Jiang; Yan-Shu Feng πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 35 KB

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: Enantioselective Ad
✍ Masanori Okaniwa; Reiko Yanada; Toshiro Ibuka πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Organoboranes for synthesis. 18. C2-symm
✍ Herbert C. Brown; Guang-Ming Chen; P. Veeraraghavan Ramachandran πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 125 KB πŸ‘ 1 views

Several new chiral auxiliaries with differing steric and electronic environments, such as ␣,␣Ј-dimethyl-2,6-pyridinedimethanol, ␣,␣Ј-ditrifluoromethyl-2,6pyridinedimethanol, ␣,␣Ј-dipentafluoroethyl-2,6-pyridinedimethanol, and ␣,␣Ј-diallyl-2,6pyridinedimethanol, have been examined and compared with ␣