The esperamicin- calicheamicin aglycones: Ring closure of a simple strained system mediated by chromium(II)-nickel(II) salts
-
Add time:08/18/2019 Source:sciencedirect.com
2,6-Diyne-4-cyclodecen-1-ol, a highly simplified and isolable monocyclic analogue of the bicyclic aglycone of esperamicins and calicheamicins, has been obtained by an intramolecular cyclocondensation of 1-iodo-1,5-diyne-3-decen-10-al mediated by chromuim (II)-nickel(II) salts.
We also recommend Trading Suppliers and Manufacturers of Esperamicin X (cas 107175-47-3). Pls Click Website Link as below: cas 107175-47-3 suppliers
Prev:Light-induced DNA cleavage by esperamicin and neocarzinostatin
Next:Studies toward the construction of the allyltrisulfide Component in esperamicin-A1 from 5-ketoshikimic acid derivatives: Part 1) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Synthesis and crystallographic analysis of a bicyclic core related to the esperamicin/calichemicin aglycones08/21/2019
- Synthesis of 2,6-dideoxy-4-S-methyl-4-thio-d-ribo-hexopyranose, a component of the esperamicin oligosaccharide08/20/2019
- Studies toward the construction of the allyltrisulfide Component in esperamicin-A1 from 5-ketoshikimic acid derivatives: Part 108/19/2019
- Light-induced DNA cleavage by esperamicin and neocarzinostatin08/17/2019
- Regular articleSolution structure of the esperamicin A1-DNA complex1☆08/16/2019
- Stereochemical studies on esperamicins: Determination of the absolute configuration of hydroxyamino sugar fragment.08/15/2019
- Stereochemical studies on esperamicin A1: A single crystal x-ray structure of thiosugar moiety08/14/2019
- Regular paperHydrophobic DNA binding of esperamicin requires conformational distortion of the host DNA08/13/2019
- Stereochemical studies on esperamicins: The absolute configuration of their bicyclic aglycone08/12/2019


