Total synthesis of (+)-taberdicatine B and (+)-tabernabovine B
Chinese Chemical Letters(2024)
摘要
The first total synthesis of (+)-taberdicatine B and (+)-tabernabovine B has been accomplished in 10 steps with 26.9% overall yield and 15 steps with 7.3% overall yield, respectively. The prominent features of this efficient synthetic strategy include the following: (1) (+)-taberdicatine B and (+)-tabernabovine B were accessed from common advanced intermediates by varying the substituents; (2) a one-pot asymmetric bromocyclization/hydrolysis was explored to assemble HPI skeleton; (3) Dieckmann condensation to form β-keto ester for the assembly of seven-membered ring; (4) an ester reduction/amide semireduction/cyclization sequence was applied to form the cage-like framework.
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关键词
Taberdicatine B,Tabernabovine B,Hexahydropyrrolo[2,3-b]indole,Asymmetric dearomatization,Total synthesis
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