Enhancing reactivity of carbonyl compounds via hydrogen-bond formation. A DFT study of the hetero-Diels-Alder reaction between butadiene derivative and acetone in chloroform.
about
Tuning the reactivity of Fe(V)(O) toward C-H bonds at room temperature: effect of waterHydrogen bonding catalysis operates by charge stabilization in highly polar Diels-Alder reactionsA mechanochemical study of the effects of compression on a Diels-Alder reaction.Water-promoted C-S bond formation reactions.
P2860
Enhancing reactivity of carbonyl compounds via hydrogen-bond formation. A DFT study of the hetero-Diels-Alder reaction between butadiene derivative and acetone in chloroform.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Enhancing reactivity of carbon ...... ive and acetone in chloroform.
@en
Enhancing reactivity of carbon ...... ive and acetone in chloroform.
@nl
type
label
Enhancing reactivity of carbon ...... ive and acetone in chloroform.
@en
Enhancing reactivity of carbon ...... ive and acetone in chloroform.
@nl
prefLabel
Enhancing reactivity of carbon ...... ive and acetone in chloroform.
@en
Enhancing reactivity of carbon ...... ive and acetone in chloroform.
@nl
P356
P1476
Enhancing reactivity of carbon ...... ive and acetone in chloroform.
@en
P304
P356
10.1021/JO030156S
P407
P577
2003-10-01T00:00:00Z