An organocatalytic Michael-cyclization cascade of 4-oxa-α,β-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral γ-lactols and trisubstituted γ-lactones.
about
Catalyst-Controlled, Enantioselective, and Diastereodivergent Conjugate Addition of Aldehydes to Electron-Deficient Olefins.An efficient lactamisation/N-acyliminium Pictet-Spengler domino strategy for the diasteroselective synthesis of polyhydroxylated quinoxalinone, β-carboline and quinazolinone derivatives.
P2860
An organocatalytic Michael-cyclization cascade of 4-oxa-α,β-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral γ-lactols and trisubstituted γ-lactones.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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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
An organocatalytic Michael-cyc ...... and trisubstituted γ-lactones.
@en
An organocatalytic Michael-cyc ...... and trisubstituted γ-lactones.
@nl
type
label
An organocatalytic Michael-cyc ...... and trisubstituted γ-lactones.
@en
An organocatalytic Michael-cyc ...... and trisubstituted γ-lactones.
@nl
prefLabel
An organocatalytic Michael-cyc ...... and trisubstituted γ-lactones.
@en
An organocatalytic Michael-cyc ...... and trisubstituted γ-lactones.
@nl
P2093
P2860
P356
P1476
An organocatalytic Michael-cyc ...... and trisubstituted γ-lactones.
@en
P2093
Hong-Yu Li
Ji-Kang Xie
Jun-Bing Lin
Peng-Fei Xu
Shi-Ming Xu
P2860
P304
P356
10.1039/C4CC09686J
P407
P577
2015-02-01T00:00:00Z