Enantiomerically homogeneous intermediates toward the synthesis of descarbamoylcalicheamicinone
Open Access
- 11 November 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (46) , 6667-6670
- https://doi.org/10.1016/s0040-4039(00)93570-6
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Total synthesis of calicheamicinone: new arrangements for actuation of the reductive cycloaromatization of aglycon congenersJournal of the American Chemical Society, 1991
- Lipase-catalyzed irreversible transesterification using enol esters: XAD-8 immobilized lipoprotein lipase-catalyzed resolution of secondary alcoholsTetrahedron Letters, 1990
- Lipase-catalyzed irreversible transesterification using enol esters: Resolution of cyanohydrins and syntheses of ethyl (R)-2-hydroxy-4-phenylbutyrate and (S)-propranololTetrahedron Letters, 1989
- A core system that simulates the cycloaromatization and DNA cleavage properties of calicheamicin-esperamicin: a correlation experimentThe Journal of Organic Chemistry, 1989
- Concise route to the calichemicin-esperamicin series: the crystal structure of an aglycone prototypeJournal of the American Chemical Society, 1988
- How mechanistically equivalent are singlet oxygen and triazolinedione?The Journal of Organic Chemistry, 1988
- Chiral synthesis via organoboranes. 14. Selective reductions. 41. Diisopinocampheylchloroborane, an exceptionally efficient chiral reducing agentJournal of the American Chemical Society, 1988
- Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketonesThe Journal of Organic Chemistry, 1983
- Oxidative formation and photochemical isomerization of spiro-epoxy-2,4-cyclohexadienonesTetrahedron Letters, 1972
- Periodate Oxidation of Phenols. IX. Oxidation of o-(omega-Hydroxyalkyl)phenols.Acta Chemica Scandinavica, 1971