A multicomponent reaction for the one-pot synthesis of 4-aza-2,3-didehydropodophyllotoxin and derivatives

scientific article published on 01 September 2002

A multicomponent reaction for the one-pot synthesis of 4-aza-2,3-didehydropodophyllotoxin and derivatives is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1021/OL0200908
P698PubMed publication ID12227745

P50authorChristophe TratratQ73124874
P2093author name stringSylviane Giorgi-Renault
Henri-Philippe Husson
P433issue19
P304page(s)3187-3189
P577publication date2002-09-01
P1433published inOrganic LettersQ2396276
P1476titleA multicomponent reaction for the one-pot synthesis of 4-aza-2,3-didehydropodophyllotoxin and derivatives
P478volume4

Reverse relations

cites work (P2860)
Q464154414-Aza-2,3-didehydropodophyllotoxins: new lignan with antitumor activity obtained from one-step synthesis
Q423908297-Methyl-9-p-tolyl-4,9-dihydro-furo[3,4-b]quinolin-1(3H)-one
Q421660687-p-Tolyl-10,11-dihydro-benzo[h]furo[3,4-b]quinolin-8(7H)-one
Q46006372A new synthetic approach to functionalize pyrimido[4,5-b]quinoline-2,4(1H,3H)-diones via a three-component one-pot reaction.
Q38878965Advancements in tetronic acid chemistry. Part 2: Use as a simple precursor to privileged heterocyclic motifs
Q80233213An efficient synthesis of pyrido[2,3-d]pyrimidine derivatives and related compounds under ultrasound irradiation without catalyst
Q33912677Anticancer properties of an important drug lead podophyllotoxin can be efficiently mimicked by diverse heterocyclic scaffolds accessible via one-step synthesis.
Q39639346Design, synthesis, and biological evaluation of the first podophyllotoxin analogues as potential vascular-disrupting agents.
Q36100169Discovery of a Series of Acridinones as Mechanism-Based Tubulin Assembly Inhibitors with Anticancer Activity
Q34313834Identification of the first inhibitor of the GBP1:PIM1 interaction. Implications for the development of a new class of anticancer agents against paclitaxel resistant cancer cells.
Q35753083N-hydroxyethyl-4-aza-didehydropodophyllotoxin derivatives as potential antitumor agents
Q34730142Natural products as leads to anticancer drugs
Q33267606Structural simplification of bioactive natural products with multicomponent synthesis: dihydropyridopyrazole analogues of podophyllotoxin
Q41474287Synthesis of Novel Functionalized 4-Aza-2,3-Didehydropodophyllotoxin Derivatives with Potential Antitumor Activity
Q33985270Synthetic and application perspectives of azapodophyllotoxins: alternative scaffolds of podophyllotoxin

Search more.