Total Synthesis, Stereochemical Revision, and Biological Reassessment of Mandelalide A: Chemical Mimicry of Intrafamily Relationships.
about
Recent Advances in Drug Discovery from South African Marine InvertebratesToward Structural Correctness: Aquatolide and the Importance of 1D Proton NMR FID ArchivingTotal Synthesis of (-)-Mandelalide A Exploiting Anion Relay Chemistry (ARC): Identification of a Type II ARC/CuCN Cross-Coupling ProtocolEnantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis.Total Synthesis and Biological Assessment of Mandelalide A.Computational Chemistry to the Rescue: Modern Toolboxes for the Assignment of Complex Molecules by GIAO NMR Calculations.Total Synthesis of Cryptocaryol A by Enantioselective Iridium-Catalyzed Alcohol C-H Allylation.New Mandelalides Expand a Macrolide Series of Mitochondrial Inhibitors.Increased Biosynthetic Gene Dosage in a Genome-Reduced Defensive Bacterial Symbiont.Polyunsaturated C-Glycosidic 4-Hydroxy-2-pyrone Derivatives: Total Synthesis Shows that Putative Orevactaene Is Likely Identical with Epipyrone A.Synthetic Access to the Mandelalide Family of Macrolides: Development of an Anion Relay Chemistry Strategy.A Two-Component Alkyne Metathesis Catalyst System with an Improved Substrate Scope and Functional Group Tolerance: Development and Applications to Natural Product Synthesis.Towards theory driven structure elucidation of complex natural products: mandelalides and coibamide A.Efficient catalytic alkyne metathesis with a fluoroalkoxy-supported ditungsten(III) complex
P2860
Q26782430-0FA3FFA8-A110-42D2-91CC-E140B76EA34EQ27301308-E9A2BAED-B686-4E02-98EE-56EFA7C3D578Q28273993-0D8AA1BD-F160-4AAB-B462-47F10D3F86D2Q34523499-B0FFB7F1-E0E9-44C2-AD4F-C2D0A8CA0B21Q38814133-6FBA572C-7C74-4209-8A77-B79DA4C6CE4CQ38894201-91D207EB-4C28-4839-814C-F6DF6648FE46Q40285034-A560D5A5-0DEB-4B52-8F7A-477935B3C99EQ42514009-CC5E2D03-06F6-4C7F-8F60-A8FDA4378E6FQ47154055-B5229F7F-A5CA-45C5-8874-B24A6D9174B8Q48359531-702F8ABA-0527-4A7F-85A2-86719B091DCCQ52372978-B56F3845-7EE5-47B6-882B-E4D8D5821A39Q53086586-57AD37B9-3F81-4D1A-A413-65BF610ECFAFQ53106870-6DE8D004-7D97-43ED-9D74-C6271B97E537Q57822022-CF7428A0-740E-48CF-8D5A-79C6248BDFF3
P2860
Total Synthesis, Stereochemical Revision, and Biological Reassessment of Mandelalide A: Chemical Mimicry of Intrafamily Relationships.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Total Synthesis, Stereochemica ...... of Intrafamily Relationships.
@ast
Total Synthesis, Stereochemica ...... of Intrafamily Relationships.
@en
type
label
Total Synthesis, Stereochemica ...... of Intrafamily Relationships.
@ast
Total Synthesis, Stereochemica ...... of Intrafamily Relationships.
@en
prefLabel
Total Synthesis, Stereochemica ...... of Intrafamily Relationships.
@ast
Total Synthesis, Stereochemica ...... of Intrafamily Relationships.
@en
P2860
P50
P356
P1476
Total Synthesis, Stereochemica ...... of Intrafamily Relationships.
@en
P2093
Berit Heggen
Conny Wirtz
P2860
P304
10416-10430
P356
10.1002/CHEM.201501491
P407
P577
2015-06-10T00:00:00Z