Toward the creation of NMR databases in chiral solvents for assignments ofrelative and absolute stereochemistry: Scope and limitation

Citation
N. Hayashi et al., Toward the creation of NMR databases in chiral solvents for assignments ofrelative and absolute stereochemistry: Scope and limitation, ORG LETT, 3(14), 2001, pp. 2249-2252
Citations number
7
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
14
Year of publication
2001
Pages
2249 - 2252
Database
ISI
SICI code
1523-7060(20010712)3:14<2249:TTCOND>2.0.ZU;2-5
Abstract
[GRAPHICS] Three additional NMR databases, 1-3, in a chiral solvent are presented. The C.21-C.38 portion of oasomycin A is used to demonstrate the scope and limi tation of the universal NMR database approach in a chiral solvent for assig nment of relative and absolute stereochemistry without degradation and/or d erivatization.