about
Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular ComplexityAcademia-industry symbiosis in organic chemistry.Why a proximity-induced Diels-Alder reaction is so fast.Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.Synthetic studies inspired by vinigrol.Diterpenoids of terrestrial origin.Strained alkenes in natural product synthesis.C-C fragmentation: origins and recent applications.Synthetic Approaches and Total Syntheses of Vinigrol, a Unique Diterpenoid.Recent progress in imidoyl radical-involved reactions.An approach to mimicking the sesquiterpene cyclase phase by nickel-promoted diene/alkyne cooligomerizationEvolution of an oxidative dearomatization enabled total synthesis of vinigrolSynthesis of highly functionalized β-aminocyclopentanecarboxylate stereoisomers by reductive ring opening reaction of isoxazolines.Total syntheses of the squalene-derived halogenated polyethers ent-dioxepandehydrothyrsiferol and armatol A via bromonium- and Lewis acid-initiated epoxide-opening cascades.A one-pot synthesis of 3-trifluoromethyl-2-isoxazolines from trifluoromethyl aldoxime.Total synthesis of vinigrol.Isovanillin derived N-(un)substituted hydroxylamines possessing an ortho-allylic group: valuable precursors to bioactive N-heterocycles.Strategy towards the enantioselective synthesis of schiglautone A.A Solid Iridium Catalyst for Diastereoselective Hydrogenation.Total Synthesis of Actinophyllic Acid.A novel synthetic approach to the bicyclo[5.3.1]undecan-11-one framework of vinigrol.Pentafulvene for the synthesis of complex natural products: total syntheses of (±)-pallambins A and B.Copper-catalyzed methylative difunctionalization of alkenes
P2860
Q29031113-25497501-E535-4ED5-9198-8CE3010200DEQ35194345-05F00525-564B-4F22-AEB0-0A65492E46C6Q36185921-6B377535-3F7B-46C7-A01A-E2A6AD46D3EAQ36186718-56699524-00E9-477C-BAF4-2231E3F49789Q37770092-8CAB3FF2-74FB-4220-98E4-3861DB9FA1A6Q37895502-ED6EE0B7-2E8C-4C00-B0D8-F00489DA2034Q38085598-F5422BD2-434D-4968-A325-EDA745186677Q38151641-45183D0D-3DC4-4A2B-9C00-E4B5559F4383Q38512416-8427D5B2-3C9F-4F03-9F82-3BB9BA1D13E9Q38731025-881102C6-098A-4B1A-AF91-27BCDE16A53BQ40618867-7B5842DB-60EB-456D-88E9-A08E7D555833Q41890012-C563B0D4-349B-4C95-9194-280EED20DD06Q41981320-58EC6A04-082D-4068-8C34-6111A33C488CQ42132498-D33A9510-052F-47EA-A838-3006D8DC307DQ42782433-69601441-22ED-4A5E-8624-45ABAA86D0AAQ42938737-69AF2FA0-4DC5-4086-8B06-5CE0C9E7E8EAQ47911248-9C0D4666-C482-4040-9196-AF2143203B9EQ48134933-7D8917E5-0117-4E32-BE04-CE591FD6BA2EQ48303585-A1881A1E-C8F2-4238-A985-FC051DFA2EAFQ48683880-89974532-96FF-4A17-A831-479CA14CF8B4Q53140155-2230DEE8-2C32-4189-B080-DEEA015BB483Q53597995-E0591096-C198-49D5-95F8-15DFC1DAA9BFQ58743618-34B379A3-9B53-44F3-ACD3-4CF48A143875
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 vinigrol.
@en
type
label
Total synthesis of vinigrol.
@en
prefLabel
Total synthesis of vinigrol.
@en
P2093
P2860
P356
P1476
Total synthesis of vinigrol.
@en
P2093
Phil S Baran
Shinji Ashida
Thomas J Maimone
P2860
P304
17066-17067
P356
10.1021/JA908194B
P407
P577
2009-12-01T00:00:00Z