Highly diastereo- and enantioselective synthesis of spirooxindole-cyclohexaneamides through N,N'-dioxide/Ni(ii)-catalyzed Diels-Alder reactions.
about
NHC-catalyzed [4+2] cycloaddition reactions for the synthesis of 3'-spirocyclic oxindoles via a C-F bond cleavage protocol.Metal-free diastereoselective construction of bridged ketal spirooxindoles via a Michael addition-inspired sequence.Diastereoselective [3 + 2] cycloaddition of 3-ylideneoxindoles with in situ generated CF2HCHN2: syntheses of CF2H-containing spirooxindoles.
P2860
Highly diastereo- and enantioselective synthesis of spirooxindole-cyclohexaneamides through N,N'-dioxide/Ni(ii)-catalyzed Diels-Alder reactions.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh
2017年學術文章
@zh-hant
name
Highly diastereo- and enantios ...... talyzed Diels-Alder reactions.
@en
Highly diastereo- and enantios ...... talyzed Diels-Alder reactions.
@nl
type
label
Highly diastereo- and enantios ...... talyzed Diels-Alder reactions.
@en
Highly diastereo- and enantios ...... talyzed Diels-Alder reactions.
@nl
prefLabel
Highly diastereo- and enantios ...... talyzed Diels-Alder reactions.
@en
Highly diastereo- and enantios ...... talyzed Diels-Alder reactions.
@nl
P2093
P2860
P50
P356
P1476
Highly diastereo- and enantios ...... talyzed Diels-Alder reactions.
@en
P2093
Hongjiang Mei
Yuhang Zhou
P2860
P304
P356
10.1039/C6CC10125A
P407
P577
2017-01-30T00:00:00Z