NMR determination of the absolute configuration of chiral 1,2- and 1,3-diols
- 30 April 2003
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 44 (21) , 4063-4065
- https://doi.org/10.1016/s0040-4039(03)00845-1
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Absolute Configuration of 1,n-Diols by NMR: The Importance of the Combined Anisotropic Effects in Bis-ArylmethoxyacetatesOrganic Letters, 2000
- Application of the modified Mosher's method to linear 1,3-diolsTetrahedron Letters, 1999
- The effect of some additives on the Stille Pd0-catalyzed cross-coupling reactionJournal of Organometallic Chemistry, 1993
- A CD method for determination of the absolute stereochemistry of acyclic glycols. 1. Application of the CD exciton chirality method to acyclic 1,3-dibenzoate systemsJournal of the American Chemical Society, 1991
- Synthesen substituierter Trimethyl(naphthyl)stannane und Tri(n-butyl)(naphthyl)stannaneJournal of Organometallic Chemistry, 1989
- Stereochemical studies on the polyene macrolide nystatin A1: the hydroxyl groups in the C-1—C-10 fragment are all-synTetrahedron Letters, 1988
- An Efficient Synthesis of Aromatic Iodides from Aromatic Carboxylic AcidsSynthetic Communications, 1988
- Stereochemical studies of the skipped-polyol polyene macrolide class: NMR studies of a tetraformylal derivative of mycoticin A and B.Tetrahedron Letters, 1987
- Stereochemical studies of polyols from the polyene macrolide lienomycinThe Journal of Organic Chemistry, 1987
- Exciton chirality method and its application to configurational and conformational studies of natural productsAccounts of Chemical Research, 1972