N,N-dichloro-2-nitrobenzenesulfonamide as the electrophilic nitrogen source for direct diamination of enones.
about
Vicinal diamino functionalities as privileged structural elements in biologically active compounds and exploitation of their synthetic chemistryCu(I)-catalyzed diamination of conjugated dienes. Complementary regioselectivity from two distinct mechanistic pathways involving Cu(II) and Cu(III) species.Methods for direct alkene diamination, new & old.Manganese (IV) oxide-catalyzed electrophilic diamination of electron-deficient alkenes provides an easy synthesis of alpha,beta-diamino acid and ketone derivatives for peptidomimetic studies.
P2860
N,N-dichloro-2-nitrobenzenesulfonamide as the electrophilic nitrogen source for direct diamination of enones.
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
N,N-dichloro-2-nitrobenzenesul ...... direct diamination of enones.
@en
N,N-dichloro-2-nitrobenzenesul ...... direct diamination of enones.
@nl
type
label
N,N-dichloro-2-nitrobenzenesul ...... direct diamination of enones.
@en
N,N-dichloro-2-nitrobenzenesul ...... direct diamination of enones.
@nl
prefLabel
N,N-dichloro-2-nitrobenzenesul ...... direct diamination of enones.
@en
N,N-dichloro-2-nitrobenzenesul ...... direct diamination of enones.
@nl
P2093
P356
P1476
N,N-dichloro-2-nitrobenzenesul ...... direct diamination of enones.
@en
P2093
Allan D Headley
Dianjun Chen
Han-Xun Wei
P304
P356
10.1021/JO030193J
P407
P577
2003-10-01T00:00:00Z