Temperature-Independent Stereocontrolled [2+2] Cycloaddition. Potential of the 2,4-Pentanediol Tether in Asymmetric Reactions as a Differential Activation Entropy Promoter
- 18 February 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (9) , 2128-2129
- https://doi.org/10.1021/ja993976o
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Diastereo-differentiating intramolecular cyclopropanations of prochiral olefins and a diazo ester linked by optically active 2,4-pentanediolTetrahedron: Asymmetry, 1997
- Axial chirality control by 2,4-pentanediol or its analogue as a simple chiral linking bridge. Highly diastereodifferentiating homocoupling of a 1-lithio-2-naphthyl etherTetrahedron: Asymmetry, 1997
- Stereoselective SynthesisPublished by Wiley ,1994
- Diastereoface differentiating peracid oxidation of the enol ether derived from cyclohexanone and 2,4-pentanediol: Preparation of optically pure 2-hydroxycyclohexanone acetalTetrahedron: Asymmetry, 1993
- Asymmetric functionalization of conformationally distinctive Cs-symmetric cis-[n.3.1] bicyclic ketones. Definition of the absolute course of enantio- and diastereodifferentiationThe Journal of Organic Chemistry, 1992
- A new aromatization of ring-A of steroids. Synthesis of estroneTetrahedron Letters, 1988
- Homogeneous asymmetric hydrogenation of functionalized ketonesJournal of the American Chemical Society, 1988
- Thermodynamic Functions of TetramethylmethaneThe Journal of Chemical Physics, 1935