Total synthesis and absolute stereochemical assignment of kibdelone C.
about
Polycyclic xanthone natural products: structure, biological activity and chemical synthesisEnantioselective total synthesis and biological evaluation of (+)-kibdelone A and a tetrahydroxanthone analogue.Approaches to polycyclic 1,4-dioxygenated xanthones. Application to total synthesis of the aglycone of IB-00208Total synthesis of clostrubin.Total Synthesis of the Aglycone of IB-00208Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A.Cascade cyclizations of acyclic and macrocyclic alkynones: studies toward the synthesis of phomactin A.Dehydrogenative coupling to enable the enantioselective total synthesis of (-)-simaomicin αSynthesis and Biological Evaluation of Kibdelone C and Its Simplified Derivatives.A soft vinyl enolization approach to α-acylvinyl anions: direct aldol/aldol condensation reactions of (E)-β-chlorovinyl ketones.A radical access to highly functionalized tetrahydroxanthones.A photo-induced C-O bond formation methodology to construct tetrahydroxanthones.Total Synthesis of Ileabethoxazole, Pseudopteroxazole, and seco-Pseudopteroxazole.Toluene dioxygenase mediated oxidation of halogen-substituted benzoate esters.Enantioselective Halolactonization Reactions using BINOL-Derived Bifunctional Catalysts: Methodology, Diversification, and Applications.Transition-metal-catalyzed intramolecular cyclization of amido(hetero)arylboronic acid aldehydes to isoquinolinones and derivatives
P2860
Q34555114-77036375-CE0C-4538-8632-404D8A118B5DQ34802270-67448154-71D0-49E4-B0CF-66E1C1EEA77EQ34847180-3B5EE5C2-BFB0-4028-BB28-122ADA909629Q35245011-8736CC27-994F-4365-84C2-55A99FA279FBQ35926534-0F21DD29-A7E3-4A90-8E8B-DEC5A30158FFQ36186718-BAAF1279-36CF-4D1A-BFF6-DC8E45A13F01Q36251694-0F34FEDD-3C92-4B2A-82EE-3115485C0381Q37216754-86B22C3B-BD3B-4209-84C4-7A016AF2AC45Q38532430-7CBAE758-9DB9-4E75-9D1C-D63CB542ABFFQ40972459-11BF39D6-3511-4BB8-AD5A-0899DB3AF3AAQ43422971-B18E7349-48D1-433B-A32B-CE27FBA9E2EDQ43716897-165C6EB4-542F-4872-9EA0-1625A045314AQ43982306-61CBF590-91C4-4CE6-B165-65F68166D1BEQ48255981-8021A317-1EB1-4061-817D-9DA8EE6C2DF5Q54337086-8CE4FDE8-F806-45C4-BE16-219C47297489Q55313028-4D0C0EAF-DC6F-4B57-9267-1D74EB1B7AADQ58841886-F2F8875B-F6D4-4408-A68A-005602CA4C94
P2860
Total synthesis and absolute stereochemical assignment of kibdelone C.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Total synthesis and absolute stereochemical assignment of kibdelone C.
@ast
Total synthesis and absolute stereochemical assignment of kibdelone C.
@en
type
label
Total synthesis and absolute stereochemical assignment of kibdelone C.
@ast
Total synthesis and absolute stereochemical assignment of kibdelone C.
@en
prefLabel
Total synthesis and absolute stereochemical assignment of kibdelone C.
@ast
Total synthesis and absolute stereochemical assignment of kibdelone C.
@en
P2093
P2860
P356
P1476
Total synthesis and absolute stereochemical assignment of kibdelone C.
@en
P2093
David L Sloman
Jeffrey W Bacon
John A Porco
P2860
P304
P356
10.1021/JA203642N
P407
P577
2011-06-15T00:00:00Z