Recent Advances in the One-Step Synthesis of Distally Fluorinated Ketones.
about
Radical aryl migration enables diversity-oriented synthesis of structurally diverse medium/macro- or bridged-rings.A remote C-C bond cleavage-enabled skeletal reorganization: Access to medium-/large-sized cyclic alkenes.Two-step conversion of carboxylic esters into distally fluorinated ketones via ring cleavage of cyclopropanol intermediates: application of sulfinate salts as fluoroalkylating reagents.Achiral Pyridine Ligand-Enabled Enantioselective Radical Oxytrifluoromethylation of Alkenes with Alcohols.1,2-Arylalkylation of N-(arylsulfonyl)acrylamides using aliphatic aldehydes as the alkyl source.1,2-Difunctionalization-type (hetero)arylation of unactivated alkenes triggered by radical addition/remote (hetero)aryl migration.Radical-Mediated 1,2-Formyl/Carbonyl Functionalization of Alkenes and Application to the Construction of Medium-Sized Rings.
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P2860
Recent Advances in the One-Step Synthesis of Distally Fluorinated Ketones.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Recent Advances in the One-Step Synthesis of Distally Fluorinated Ketones.
@en
type
label
Recent Advances in the One-Step Synthesis of Distally Fluorinated Ketones.
@en
prefLabel
Recent Advances in the One-Step Synthesis of Distally Fluorinated Ketones.
@en
P2860
P356
P1476
Recent Advances in the One-Step Synthesis of Distally Fluorinated Ketones.
@en
P2093
P2860
P356
10.1002/CHEM.201504036
P407
P50
P577
2015-12-22T00:00:00Z