Highly stereoselective synthesis of beta-lactams utilizing alpha-chloroimines as new and powerful chiral inductors.
about
α-Haloaldehydes: versatile building blocks for natural product synthesis.Schiff bases: a short survey on an evergreen chemistry tool.Stereoselective synthesis of trans- and cis-2-aryl-3-(hydroxymethyl)aziridines through transformation of 4-aryl-3-chloro-beta-lactams and study of their ring opening.Mechanistic insight into the regioselectivity of Pd(ii)-catalyzed C-H functionalization of N-methoxy cinnamamide.
P2860
Highly stereoselective synthesis of beta-lactams utilizing alpha-chloroimines as new and powerful chiral inductors.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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name
Highly stereoselective synthes ...... and powerful chiral inductors.
@en
Highly stereoselective synthes ...... and powerful chiral inductors.
@nl
type
label
Highly stereoselective synthes ...... and powerful chiral inductors.
@en
Highly stereoselective synthes ...... and powerful chiral inductors.
@nl
prefLabel
Highly stereoselective synthes ...... and powerful chiral inductors.
@en
Highly stereoselective synthes ...... and powerful chiral inductors.
@nl
P2093
P2860
P356
P1476
Highly stereoselective synthes ...... and powerful chiral inductors.
@en
P2093
Matthias D'hooghe
Stijn Dekeukeleire
Willem Van Brabandt
Yves Dejaegher
P2860
P304
P356
10.1002/CHEM.200800845
P407
P577
2008-01-01T00:00:00Z