10183-93-4Relevant articles and documents
Berlin et al.
, (1972)
Version: 1.0
Creation Date: Aug 15, 2017
Revision Date: Aug 15, 2017
Product name | (2S,3R)-3-[(1S,3S,4R)-3,4-dihydroxy-1-methoxy-2-oxopentyl]-2,6,8,9-tetrahydroxy-7-methyl-3,4-dihydro-2H-anthracen-1-one |
---|
Product number | - |
---|---|
Other names | Chromomycin-B |
Identified uses | For industry use only. |
---|---|
Uses advised against | no data available |
Emergency phone number | - |
---|---|
Service hours | Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours). |
More Details:10183-93-4 SDS
The palladium catalyzed homogeneous reduction of a variety of phenols with either sodium borohydride or triethylammonium formate are effected as their triflate esters. This transformation extends the usefulness of the benzannulation reaction of chromium carbene complexes with acetylenes and is e...detailed
Appropriate dithiane derivatives of D-threo configuration were prepared starting with D-arabinose and D-galactose, respectively. Their dianions served for nucleophilic additions to model aldehydes, thus comprising syntheses of the complex side chain of chromomycinone. In contrast to former repor...detailed
It has been shown that chromomycinone can be represented by the absolute configurational structure 1. Molecular rotation differences between the acetate and benzoate of secondary alcohols can be employed for deriving the absolute configuration.detailed
The various reactions of chromomycinone, the chromophore of the cancerostatic chromomycins, are described. The structures of several chromomycinone derivatives are also discussed.detailed