about
Total synthesis of maoecrystal V: early-stage C-H functionalization and lactone assembly by radical cyclizationReactivity and chemoselectivity of allenes in Rh(I)-catalyzed intermolecular (5 + 2) cycloadditions with vinylcyclopropanes: allene-mediated rhodacycle formation can poison Rh(I)-catalyzed cycloadditionsA Convenient Reagent for Aldehyde to Alkyne Homologation.Toward the Ideal Synthesis and Transformative Therapies: The Roles of Step Economy and Function Oriented Synthesis.Chemistry of polyvalent iodine.3-Acyloxy-1,4-enyne: a New Five-carbon Synthon for Rhodium-Catalyzed (5+2) CycloadditionsTotal synthesis of (+)-asteriscanolide: further exploration of the rhodium(I)-catalyzed [(5+2)+1] reaction of ene-vinylcyclopropanes and CO.Pseudolaric acid B attenuates atopic dermatitis-like skin lesions by inhibiting interleukin-17-induced inflammation.Rhodium-catalyzed intra- and intermolecular [5 + 2] cycloaddition of 3-acyloxy-1,4-enyne and alkyne with concomitant 1,2-acyloxy migrationA unified approach to the daucane and sphenolobane bicyclo[5.3.0]decane core: enantioselective total syntheses of daucene, daucenal, epoxydaucenal B, and 14-para-anisoyloxydauc-4,8-diene.Rhodium-Catalyzed Stereoselective Intramolecular [5 + 2] Cycloaddition of 3-Acyloxy 1,4-Enyne and Alkene.Synthesis of (+)-schisanwilsonene A by tandem gold-catalyzed cyclization/1,5-migration/cyclopropanation.Copper Catalysis and Organocatalysis Showing the Way: Synthesis of Selenium-containing Highly Functionalized 1,2,3-Triazoles.Cationic rhodium(I)-catalyzed regioselective tandem heterocyclization/[3+2] cycloaddition of 2-(1-alkynyl)-2-alken-1-ones with alkynes.Pseudolaric acid B-driven phosphorylation of c-Jun impairs its role in stabilizing HIF-1alpha: a novel function-converter model.
P2860
Q28298731-1FCD31B6-142B-453F-B184-08A0D0A8B6DFQ34778278-BA3E1246-2BCC-485D-96FF-28B075607F58Q37080251-14C94EA2-56B8-40F7-8BE0-A332DBCE3342Q37095319-E5EF6E8B-4285-416F-939F-4075CEB9215CQ37318116-2182278E-E435-4001-ABBD-927B24E3428CQ39629689-1F5B4856-9CF3-446A-B295-00962354374DQ39667214-6CE52A26-A550-4AB3-A046-A6C365C6C2F8Q41366939-1B558C7B-7F71-452F-95F3-4325D05A1095Q41888010-01C8B566-0D0C-4566-B752-69DA9C64B795Q41962514-7D885522-A3D9-41C4-B0B1-B5BAA2F96EB7Q42141369-FFB587E6-B7B1-4F2E-9B34-CCB018FDE65EQ48009101-0270A477-51FB-4240-A73B-60EC4A09D89FQ49865005-8AA941CF-D18A-4FA3-AEBC-EDAD9D6649F9Q50502783-80381116-9EA0-4690-9489-CA1B11710C88Q54319778-1F6C7354-ACAE-42DC-B9F9-812E4A4035ED
P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
name
Total synthesis of (-)-pseudolaric acid B
@ast
Total synthesis of (-)-pseudolaric acid B
@en
type
label
Total synthesis of (-)-pseudolaric acid B
@ast
Total synthesis of (-)-pseudolaric acid B
@en
prefLabel
Total synthesis of (-)-pseudolaric acid B
@ast
Total synthesis of (-)-pseudolaric acid B
@en
P2860
P356
P1476
Total synthesis of (-)-pseudolaric acid B
@en
P2093
Arndt Meyer
P2860
P304
14556-14557
P356
10.1021/JA076165Q
P407
P577
2007-11-07T00:00:00Z