about
Alkyne elementometalation-Pd-catalyzed cross-coupling. Toward synthesis of all conceivable types of acyclic alkenes in high yields, efficiently, selectively, economically, and safely: "green" wayDevelopment of a general, sequential, ring-closing metathesis/intramolecular cross-coupling reaction for the synthesis of polyunsaturated macrolactonesAlkyne metathesis: development of a novel molybdenum-based catalyst system and its application to the total synthesis of epothilone A and C.Phosphate tether-mediated approach to the formal total synthesis of (-)-salicylihalamides A and B.Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.Evaluating the potential of vacuolar ATPase inhibitors as anticancer agents and multigram synthesis of the potent salicylihalamide analog saliphenylhalamide.Impact of copper-catalyzed cross-coupling reactions in natural product synthesis: the emergence of new retrosynthetic paradigms.Cu-mediated enamide formation in the total synthesis of complex peptide natural products.Synthesis and biological evaluation of a potent salicylihalamide A lactam analogue.Molecular editing and assessment of the cytotoxic properties of iejimalide and progeny.Gram-scale synthesis of iejimalide B.Preparation, modification, and evaluation of cruentaren A and analogues.A fluorous-tagged linker from which small molecules are released by ring-closing metathesisSynthesis of the entire framework of tartrolon B utilizing a silicon-tethered ring-closing metathesis strategy.Increasing the structural span of alkyne metathesis.A total synthesis of spirastrellolide A methyl ester.Anisotropic ionic conductivity in fluorinated ionic liquid crystals suitable for optoelectronic applications
P2860
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P2860
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Total synthesis of (-)-salicylihalamide.
@en
type
label
Total synthesis of (-)-salicylihalamide.
@en
prefLabel
Total synthesis of (-)-salicylihalamide.
@en
P2093
P2860
P1476
Total synthesis of (-)-salicylihalamide.
@en
P2093
P2860
P304
P356
10.1002/1521-3765(20011217)7:24<5286::AID-CHEM5286>3.0.CO;2-G
P407
P577
2001-12-01T00:00:00Z