Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
about
Characterization of DNA damage induced by a natural product antitumor antibiotic leinamycin in human cancer cells.The macrocycle of leinamycin imparts hydrolytic stability to the thiol-sensing 1,2-dithiolan-3-one 1-oxide unit of the natural productSynthesis and characterization of a small analogue of the anticancer natural product leinamycin.Evidence for a Morin type intramolecular cyclization of an alkene with a phenylsulfenic acid group in neutral aqueous solution
P2860
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
description
2007 nî lūn-bûn
@nan
2007 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
@ast
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
@en
type
label
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
@ast
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
@en
prefLabel
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
@ast
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
@en
P2860
P356
P1476
Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides
@en
P2093
Kent S Gates
Kripa Keerthi
P2860
P304
P356
10.1039/B701179B
P577
2007-04-13T00:00:00Z