数据链接：
官方服务：
资源简介：
Asymmetric Total Synthesis of Vindoline
应用场景：
创建时间：
2010-03-24
相关数据集
Chemoenzymatic Total Syntheses of Ribisins A, B, and D, Polyoxygenated Benzofuran Derivatives Displaying NGF-Potentiating Properties
Total syntheses of the structures, 1, 2, and 4, assigned to the biologically active natural products ribisins A, B, and D, respectively, have been achieved using the microbially derived and enantiomer
NIAID Data Ecosystem70
Total Synthesis and Biological Evaluation of Leptosphaerone B and Derivatives of Microketide A
Microketide A and B are fungal polyketides reported to display potent activity against Gram-negative pathogens, yet the lack of synthetic access has prevented detailed investigation of their mode of a
NIAID Data Ecosystem30
Syntheses of (+)-30- epi -, (−)-6- epi ‑, (±)-6,30- epi -13,14-Didehydroxyisogarcinol and (±)-6,30- epi -Garcimultiflorone A Utilizing Highly Diastereoselective, Lewis Acid-Controlled Cyclizations
The first syntheses of 13,14-didehydroxyisogarcinol (6) and garcimultiflorone A (5) stereoisomers are reported in six steps from a commercially available phloroglucinol. Lewis acid-controlled, diaster
NIAID Data Ecosystem20
Scalable Synthesis of (−)-Thapsigargin
Total syntheses of the complex, highly oxygenated sesquiterpenes thapsigargin (1) and nortrilobolide (2) are presented. Access to analogues of these promising bioactive natural products has been limit
NIAID Data Ecosystem60
Broadly Applicable Stereoselective Syntheses of Serrulatane, Amphilectane Diterpenes, and Their Diastereoisomeric Congeners Using Asymmetric Hydrovinylation for Absolute Stereochemical Control
A stereogenic center, placed at an exocyclic location next to a chiral carbon in a ring to which it is attached, is a ubiquitous structural motif seen in many bioactive natural products, including di-
NIAID Data Ecosystem30
