Synthesis of strained tricyclic beta-lactams by intramolecular [2+2] cycloaddition reactions of 2-azetidinone-tethered enallenols: control of regioselectivity by selective alkene substitution.
about
Exploiting [2+2] cycloaddition chemistry: achievements with allenes.Allenyl-β-lactams: versatile scaffolds for the synthesis of heterocycles.Synthesis of substituted tetrahydrocyclobuta[b]benzofurans by palladium-catalyzed substitution/[2+2] cycloaddition of propargylic carbonates with 2-vinylphenols.Recent developments in the synthesis of condensed β-lactams
P2860
Synthesis of strained tricyclic beta-lactams by intramolecular [2+2] cycloaddition reactions of 2-azetidinone-tethered enallenols: control of regioselectivity by selective alkene substitution.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Synthesis of strained tricycli ...... selective alkene substitution.
@en
Synthesis of strained tricycli ...... selective alkene substitution.
@nl
type
label
Synthesis of strained tricycli ...... selective alkene substitution.
@en
Synthesis of strained tricycli ...... selective alkene substitution.
@nl
prefLabel
Synthesis of strained tricycli ...... selective alkene substitution.
@en
Synthesis of strained tricycli ...... selective alkene substitution.
@nl
P2093
P356
P1476
Synthesis of strained tricycli ...... selective alkene substitution.
@en
P2093
Cristina Aragoncillo
M Rosario Torres
María C Redondo
P2860
P304
P356
10.1002/CHEM.200500807
P407
P577
2006-02-01T00:00:00Z