Emulating the logic of monoterpenoid alkaloid biogenesis to access a skeletally diverse chemical library.
about
Catalytic asymmetric α-Iminol rearrangement: new chiral platformsBiosynthetically inspired divergent approach to monoterpene indole alkaloids: total synthesis of mersicarpine, leuconodines B and D, leuconoxine, melodinine E, leuconolam, and rhazinilam.Divergent Synthesis of Hydro-γ-Carbolines and Multisubstituted Indoles through Grob Fragmentation/Mannich Cyclization.A core switching strategy to pyrrolo[2,3-b]quinolines and diazocino[1,2-a]indolinones.Hydrogen-Bonding Network Promoted [3+2] Cycloaddition: Asymmetric Catalytic Construction of Spiro-pseudoindoxyl Derivatives.
P2860
Emulating the logic of monoterpenoid alkaloid biogenesis to access a skeletally diverse chemical library.
description
2013 nî lūn-bûn
@nan
2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Emulating the logic of monoter ...... ally diverse chemical library.
@ast
Emulating the logic of monoter ...... ally diverse chemical library.
@en
Emulating the logic of monoter ...... ally diverse chemical library.
@nl
type
label
Emulating the logic of monoter ...... ally diverse chemical library.
@ast
Emulating the logic of monoter ...... ally diverse chemical library.
@en
Emulating the logic of monoter ...... ally diverse chemical library.
@nl
prefLabel
Emulating the logic of monoter ...... ally diverse chemical library.
@ast
Emulating the logic of monoter ...... ally diverse chemical library.
@en
Emulating the logic of monoter ...... ally diverse chemical library.
@nl
P2093
P2860
P356
P1476
Emulating the logic of monoter ...... ally diverse chemical library.
@en
P2093
John S Scotti
Sergey A Kozmin
P2860
P304
P356
10.1021/JO401262V
P407
P577
2013-08-27T00:00:00Z