Asymmetric induction in mixed [2 + 2] photoadditions employing a chiral auxiliary in the alkene component
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (50) , 6163-6166
- https://doi.org/10.1016/s0040-4039(00)95042-1
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Asymmetric Diels‐Alder and Ene Reactions in Organic Synthesis. New Synthetic Methods (48)Angewandte Chemie International Edition in English, 1984
- The determination of absolute configuration using nuclear magnetic resonance techniquesProgress in Nuclear Magnetic Resonance Spectroscopy, 1982
- High Asymmetric Induction in Conjugate Additions of RCu · BF3 to Chiral Enoates. Preliminary communicationHelvetica Chimica Acta, 1981
- Asymmetric induction in Diels‐Alder reactions to acrylates derived from chiral sec‐alcohols. Preliminary communicationHelvetica Chimica Acta, 1981
- Enantiomerically pure lactones. 3. Synthesis of and stereospecific conjugate additions to .alpha.,.beta.-unsaturated lactonesThe Journal of Organic Chemistry, 1980
- Santolinolide B [(2R,3S,4S)-4-hydroxy-2,5-dimethyl-3-vinyl-5-hexenoic acid lactone]. A new irregular monoterpene from Artemisia tridentata tridentataThe Journal of Organic Chemistry, 1979
- The use of chiral solvating agent for nuclear magnetic resonance determination of enantiomeric purity and absolute configuration of lactones. Consequences of three-point interactionsThe Journal of Organic Chemistry, 1977
- Nuclear magnetic resonance determination of enantiomeric composition and absolute configuration of .gamma.-lactones using chiral 2,2,2-trifluoro-1-(9-anthryl)ethanolThe Journal of Organic Chemistry, 1977