Splitting a Substrate into Three Parts: Gold-Catalyzed Nitrogenation of Alkynes by C-C and C≡C Bond Cleavage.
about
Recent advances in the tandem reaction of azides with alkynes or alkynols.Silver-Catalyzed Stereoselective Aminosulfonylation of Alkynes.AgNO3 as nitrogen source for rhodium(iii)-catalyzed synthesis of 2-aryl-2H-benzotriazoles from azobenzenes.[3+2] Cycloaddition of azide with aldehyde hydrazone through an aminyl radical-polar crossover strategy.Thiazolium salt-catalyzed C-C triple bond cleavage for accessing substituted 1-naphthols via benzannulation.α-Substituted vinyl azides: an emerging functionalized alkene.tert-Butyl nitrite (TBN) as the N atom source for the synthesis of substituted cinnolines with 2-vinylanilines and a relevant mechanism was studied.Electronic halocyclization and radical haloazidation of benzene-linked 1,7-dienes for the synthesis of functionalized 3,1-benzoxazines.Copper(i)-catalysed oxidative C-N coupling of 2-aminopyridine with terminal alkynes featuring a C[triple bond, length as m-dash]C bond cleavage promoted by visible light.
P2860
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P2860
Splitting a Substrate into Three Parts: Gold-Catalyzed Nitrogenation of Alkynes by C-C and C≡C Bond Cleavage.
description
2015 nî lūn-bûn
@nan
2015年の論文
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2015年学术文章
@wuu
2015年学术文章
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2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
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2015年學術文章
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2015年學術文章
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name
Splitting a Substrate into Thr ...... by C-C and C≡C Bond Cleavage.
@en
Splitting a Substrate into Thr ...... by C-C and C≡C Bond Cleavage.
@nl
type
label
Splitting a Substrate into Thr ...... by C-C and C≡C Bond Cleavage.
@en
Splitting a Substrate into Thr ...... by C-C and C≡C Bond Cleavage.
@nl
prefLabel
Splitting a Substrate into Thr ...... by C-C and C≡C Bond Cleavage.
@en
Splitting a Substrate into Thr ...... by C-C and C≡C Bond Cleavage.
@nl
P2093
P2860
P356
P1476
Splitting a Substrate into Thr ...... by C-C and C≡C Bond Cleavage.
@en
P2093
P2860
P304
P356
10.1002/ANIE.201508347
P407
P577
2015-10-23T00:00:00Z