Improved Conditions for Facile Overman Rearrangement(1).

Improved Conditions for Facile Overman Rearrangement(1).

Item
http://www.wikidata.org/entity/Q33955640
Stereoselective synthesis of the eastern quinolizidine portion of himeradine A.Asymmetric Synthesis of (+)-Iso-6-Cassine via Stereoselective Intramolecular Amidomercuration.Recent advances in the Overman rearrangement: synthesis of natural products and valuable compounds.Expanding stereochemical and skeletal diversity using petasis reactions and 1,3-dipolar cycloadditions.Highly efficient gold(I)-catalyzed Overman rearrangement in water.A facile synthesis of cis-4-amino-2-cyclopentene-1-methanol, a key intermediate for the synthesis of carbocyclic nucleosides.Cascade- and orthoamide-type Overman rearrangements of allylic vicinal diols.Microwave accelerated aza-Claisen rearrangement.Synthesis of tetrodotoxin, a classic but still fascinating natural product.Enantioselective Total Synthesis of (+)-Neostenine.The Allylic Trihaloacetimidate RearrangementA new general approach for the stereocontrolled synthesis of functionalised γ- and δ-lactams
P2860

Improved Conditions for Facile Overman Rearrangement(1).

Item
http://www.wikidata.org/entity/Q33955640
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Improved Conditions for Facile Overman Rearrangement(1).
@ast
Improved Conditions for Facile Overman Rearrangement(1).
@en
type
label
Improved Conditions for Facile Overman Rearrangement(1).
@ast
Improved Conditions for Facile Overman Rearrangement(1).
@en
prefLabel
Improved Conditions for Facile Overman Rearrangement(1).
@ast
Improved Conditions for Facile Overman Rearrangement(1).
@en
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P577
P698
P356
P1433
P1476
Improved Conditions for Facile Overman Rearrangement(1).
@en
P2093
P304
P31
P356
P407
P433
P478
P577
P698