Groebke multicomponent reaction and subsequent nucleophilic aromatic substitution for a convenient synthesis of 3,8-diaminoimidazo[1,2-a]pyrazines as potential kinase inhibitors.
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Multi-substituted 8-aminoimidazo[1,2-a]pyrazines by Groebke-Blackburn-Bienaymé reaction and their Hsp90 inhibitory activityRecent advances in development of imidazo[1,2-a]pyrazines: synthesis, reactivity and their biological applications.Groebke-Blackburn-Bienaymé multicomponent reaction: emerging chemistry for drug discovery.Chemoselective preparation of 1,2,3-triazole-isoxazole bisfunctional derivatives and their application in peptidomimetic synthesis.
P2860
Groebke multicomponent reaction and subsequent nucleophilic aromatic substitution for a convenient synthesis of 3,8-diaminoimidazo[1,2-a]pyrazines as potential kinase inhibitors.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-my
2011年学术文章
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2011年學術文章
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2011年學術文章
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2011年學術文章
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name
Groebke multicomponent reactio ...... s potential kinase inhibitors.
@en
Groebke multicomponent reactio ...... s potential kinase inhibitors.
@nl
type
label
Groebke multicomponent reactio ...... s potential kinase inhibitors.
@en
Groebke multicomponent reactio ...... s potential kinase inhibitors.
@nl
prefLabel
Groebke multicomponent reactio ...... s potential kinase inhibitors.
@en
Groebke multicomponent reactio ...... s potential kinase inhibitors.
@nl
P2093
P2860
P50
P356
P1476
Groebke multicomponent reactio ...... as potential kinase inhibitors
@en
P2093
Antonio Caldarelli
Gian Cesare Tron
Giovanni Sorba
Margherita Guasconi
Tracey Pirali
Xiaoyun Lu
P2860
P304
P356
10.1039/C1OB05336A
P577
2011-04-14T00:00:00Z