Understanding the nature of the molecular mechanisms associated with the competitive Lewis acid catalyzed [4+2] and [4+3] cycloadditions between arylidenoxazolone systems and cyclopentadiene: a DFT analysis.
about
Stereoselectivities and regioselectivities of (4 + 3) cycloadditions between allenamide-derived chiral oxazolidinone-stabilized oxyallyls and furans: experiment and theory.Regioselectivities of (4 + 3) cycloadditions between furans and oxazolidinone-substituted oxyallyls.Theoretical study on the molecular mechanism of the [5 + 2] vs. [4 + 2] cyclization mediated by Lewis acid in the quinone system.
P2860
Understanding the nature of the molecular mechanisms associated with the competitive Lewis acid catalyzed [4+2] and [4+3] cycloadditions between arylidenoxazolone systems and cyclopentadiene: a DFT analysis.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
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name
Understanding the nature of th ...... clopentadiene: a DFT analysis.
@en
Understanding the nature of th ...... clopentadiene: a DFT analysis.
@nl
type
label
Understanding the nature of th ...... clopentadiene: a DFT analysis.
@en
Understanding the nature of th ...... clopentadiene: a DFT analysis.
@nl
prefLabel
Understanding the nature of th ...... clopentadiene: a DFT analysis.
@en
Understanding the nature of th ...... clopentadiene: a DFT analysis.
@nl
P356
P1476
Understanding the nature of th ...... clopentadiene: a DFT analysis.
@en
P2093
M Teresa Picher
Manuel Arnó
P304
P356
10.1002/CHEM.200400277
P407
P577
2004-10-01T00:00:00Z