A new framework for the cycloaromatization of enediynes under mild conditions
- 11 August 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (32) , 5583-5586
- https://doi.org/10.1016/s0040-4039(97)01263-x
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- The chemistry of enediynes, enyne allenes and related compoundsTetrahedron, 1996
- The enediyne and dienediyne based antitumour antibiotics. Methodology and strategies for total synthesis and construction of bioactive analogues. Part 2Contemporary Organic Synthesis, 1996
- The enediyne and dienediyne based antitumour antibiotics. Methodology and strategies for total synthesis and construction of bioactive analogues. Part 1Contemporary Organic Synthesis, 1996
- Lactendiynes: A New Class of Triggered Cyclic EnediynesAngewandte Chemie International Edition in English, 1995
- Design of Enediyne ProdrugsSynlett, 1995
- Synthetic and mechanistic studies on esperamicin A1 and calichemicin .gamma.1. Molecular strain rather than .pi.-bond proximity determines the cycloaromatization rates of bicyclo[7.3.1]enediynesJournal of the American Chemical Society, 1990
- Monocyclic enediyne collapse to 1,4-diyl biradicals: a pathway under strain controlJournal of the American Chemical Society, 1990
- Characterization of the in vitro cyclization chemistry of calicheamicin and its relation to DNA cleavageJournal of the American Chemical Society, 1990
- The cyclization of calichemicin-esperamicin analogs: a predictive biradicaloid transition stateJournal of the American Chemical Society, 1989
- Cyclic conjugated enediynes related to calicheamicins and esperamicins: calculations, synthesis, and propertiesJournal of the American Chemical Society, 1988