Callipeltoside a: total synthesis, assignment of the absolute and relative configuration, and evaluation of synthetic analogues.
about
Total synthesis of (-)-callipeltoside ASame data, different structures: diastereoisomers with substantially identical NMR data from nature.The taumycin A macrocycle: asymmetric total synthesis and revision of relative stereochemistry.Natural products from the Lithistida: a review of the literature since 2000.Rhodium-Catalyzed C-H Amination - An Enabling Method for Chemical Synthesis.Regiodivergent addition of phenols to allylic oxides: control of 1,2- and 1,4-additions for cyclitol synthesis.Metal Catalyzed Allylic Alkylation: Its Development in the Trost LaboratoriesDual macrolactonization/pyran-hemiketal formation via acylketenes: applications to the synthesis of (-)-callipeltoside A and a lyngbyaloside B model system.Catalytic Asymmetric Synthesis of Branched Chiral Allylic Phenyl Ethers from (E)-Allylic Alcohols.INTEGRATED APPROACHES TO THE CONFIGURATIONAL ASSIGNMENT OF MARINE NATURAL PRODUCTSA stereoselective synthesis of the bromopyrrole natural product (-)-agelastatin A.Bond formations by intermolecular and intramolecular trappings of acylketenes and their applications in natural product synthesis.Diastereotopos-differentiating C-H activation reactions at methylene groups.Natural glycoconjugates with antitumor activity.Phosphino-carboxamides: the inconspicuous gems.Catalytic asymmetric synthesis of allylic alcohols and derivatives and their applications in organic synthesis.Advances in the total synthesis of biologically important callipeltosides: a review.Ester coupling reactions--an enduring challenge in the chemical synthesis of bioactive natural products.O-Glycosylation methods in the total synthesis of complex natural glycosides.Stereoselective Halogenation in Natural Product Synthesis.Total synthesis and structural revision of callipeltoside C.Enantioselective total synthesis of callipeltoside A: two approaches to the macrolactone fragmentCallipeltosides A, B and C: Total Syntheses and Structural Confirmation.Metallacycle-Mediated Cross-Coupling in Natural Product Synthesis.Highly stereoselective cyclopropanation of α,β-unsaturated carbonyl compounds with methyl (diazoacetoxy)acetate catalyzed by a chiral ruthenium(II) complex.Transition metal-catalyzed iodine(iii)-mediated nitrene transfer reactions: efficient tools for challenging syntheses.Atom-Economical Dimerization Strategy by the Rhodium-Catalyzed Addition of Carboxylic Acids to Allenes: Protecting-Group-Free Synthesis of Clavosolide A and Late-Stage Modification.Formation of Chiral Allylic Ethers via an Enantioselective Palladium-Catalyzed Alkenylation of Acyclic Enol Ethers.Convergent Total Syntheses of Callipeltosides A, B, and C
P2860
Q30498592-BAAA170B-3D76-4813-A9B1-4B1379092915Q31028526-AC2B1223-19D1-4B72-920A-CE22233D015FQ34285982-A0915B4A-2FC9-4A2D-82E6-440F82EC6DE0Q34636153-5B82EA15-EE40-42DB-8C9B-FCE23ADAA5C3Q35127763-27DBCEA3-BD49-487A-9CDE-5DC1A84F891FQ35141845-E0E9EC2A-F6B6-4A4A-BA8A-BAF8EF6CCD76Q35895833-56790C13-F3A6-4E90-8162-40F817628763Q36128295-1E6BFBC2-8F0C-4953-ABC6-FDAA7766C0E0Q36946139-C46E8959-9F6E-49DF-9C51-857637181FFAQ36960591-4001D439-FA42-4804-B430-34CBA05F5D5BQ37469470-8DD02856-3FAC-4842-8245-B5A38D231A9FQ37619252-A7D07166-3229-41C8-8702-9D8AA512DEFDQ37809754-00292524-0D1B-4500-AFC2-7A60D882F297Q37814157-5578C6E5-9665-44DF-9C4F-F51D6568102BQ37997959-1122F3D9-65D4-46E6-A8D1-306D2775B898Q38074104-D550D159-3DD3-4CB9-A4C2-86BBF3C8436FQ38090958-268ED86A-BBC6-476A-B7A4-B5598D05DFEFQ38311744-6194D727-DAC9-4D8B-800F-E5EC9137EDC2Q38525726-AF8D766D-B4D0-41A6-96D3-352E4E514900Q38718959-F462167E-AC79-4215-808B-22D8C07BD88BQ41554909-B6BF79EA-603D-4588-B6C4-F30CB45A9E86Q42256309-ADE9701F-7925-45C1-96EA-72F40A4E8FBEQ43239492-04982E94-CDCD-401F-AF5E-655C5B48D66BQ43267324-0E2CAEA0-F931-46C9-96F6-36AE26375961Q45344825-48F55A8C-F5C4-4C94-B938-55BDAB96C069Q48184302-ADFB33FC-B36E-4B00-9479-F64C0F95E512Q50914346-7E1B5355-48C2-45DF-A496-45E482E38E0AQ55175991-BC5D0EDA-E624-4CDB-9981-02957ADB2B79Q56951764-8E58D233-9C6D-4843-A3A5-763BEF7EE997
P2860
Callipeltoside a: total synthesis, assignment of the absolute and relative configuration, and evaluation of synthetic analogues.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Callipeltoside a: total synthe ...... uation of synthetic analogues.
@en
Callipeltoside a: total synthe ...... uation of synthetic analogues.
@nl
type
label
Callipeltoside a: total synthe ...... uation of synthetic analogues.
@en
Callipeltoside a: total synthe ...... uation of synthetic analogues.
@nl
prefLabel
Callipeltoside a: total synthe ...... uation of synthetic analogues.
@en
Callipeltoside a: total synthe ...... uation of synthetic analogues.
@nl
P2093
P356
P1476
Callipeltoside a: total synthe ...... uation of synthetic analogues.
@en
P2093
Janet L Gunzner
Olivier Dirat
Young H Rhee
P304
10396-10415
P356
10.1021/JA0205232
P407
P50
P577
2002-09-01T00:00:00Z