about
A macrocyclic β-iodoallenolate intermediate is key: synthesis of the ABD core of phomactin A.Gold (III) Chloride-Catalyzed 6-endo-trig Oxa-Michael Addition Reactions for Diastereoselective Synthesis of Fused Tetrahydropyranones.Ether-directed ortho-C-H olefination with a palladium(II)/monoprotected amino acid catalyst.Cascade cyclizations of acyclic and macrocyclic alkynones: studies toward the synthesis of phomactin A.Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products.Total synthesis of (±)-phomactin A. Lessons learned from respecting a challenging structural topology.Total Syntheses of Proposed (±)-Trichodermatides B and C.Constructing the Architecturally Distinctive ABD-Tricycle of Phomactin A through an Intramolecular Oxa-[3 + 3] Annulation Strategy.Carbocyclization cascades of allyl ketenimines via aza-Claisen rearrangements of N-phosphoryl-N-allyl-ynamides.Organocatalytic Intramolecular [4+2] Cycloaddition between In Situ Generated Vinylidene ortho-Quinone Methides and Benzofurans.
P2860
Q36251694-8FF383F8-E546-46FB-8EC9-27A0777C8B33Q37156765-CBF2FFF9-6CE1-40E7-AFEC-F5684E9641D5Q37206766-5F2BD13E-D3EA-451C-9457-50EE761444DCQ37216754-3B243EA2-4926-4042-8DBA-FF5DF926C8DAQ38181092-D9A7EFF7-6FA0-40A2-A25E-31146F498A5EQ38267093-4A3DF477-41AF-4BD9-92EF-C5FA172CE869Q42136625-A0D52066-34BF-4C28-8D6A-5704EE349DC1Q42145217-98D65FFD-DCED-4BDC-9BCE-9319FE3738F0Q42554645-E44C47D7-7986-40ED-8E38-F47D45F43429Q48133065-2F1DA65B-6C3B-40EA-A8B3-0876B068E531
P2860
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Total synthesis of phomactin A.
@en
type
label
Total synthesis of phomactin A.
@en
prefLabel
Total synthesis of phomactin A.
@en
P2093
P2860
P356
P1433
P1476
Total synthesis of phomactin A.
@en
P2093
Grant S Buchanan
Kevin P Cole
Richard P Hsung
P2860
P304
P356
10.1021/OL900237E
P407
P577
2009-04-01T00:00:00Z