Rapid and stereocontrolled synthesis of racemic and optically pure highly functionalized pyrrolizidine systems via rearrangement of 1,3-dipolar cycloadducts derived from 2-azetidinone-tethered azomethine ylides.
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Stereoselective Synthesis of Quaternary Proline Analogues.Additions of allenyl/propargyl organometallic reagents to 4-oxoazetidine-2-carbaldehydes: novel palladium-catalyzed domino reactions in allenynes.Synthetically useful noncatalytic strategy: a stereocontrolled rapid cyclization of a three component system to afford hexahydropyrrolizines.Michael addition/pericyclization/rearrangement--a multicomponent strategy for the synthesis of substituted resorcinols.
P2860
Rapid and stereocontrolled synthesis of racemic and optically pure highly functionalized pyrrolizidine systems via rearrangement of 1,3-dipolar cycloadducts derived from 2-azetidinone-tethered azomethine ylides.
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年学术文章
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2001年學術文章
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2001年學術文章
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name
Rapid and stereocontrolled syn ...... ne-tethered azomethine ylides.
@en
Rapid and stereocontrolled syn ...... ne-tethered azomethine ylides.
@nl
type
label
Rapid and stereocontrolled syn ...... ne-tethered azomethine ylides.
@en
Rapid and stereocontrolled syn ...... ne-tethered azomethine ylides.
@nl
prefLabel
Rapid and stereocontrolled syn ...... ne-tethered azomethine ylides.
@en
Rapid and stereocontrolled syn ...... ne-tethered azomethine ylides.
@nl
P356
P1476
Rapid and stereocontrolled syn ...... ne-tethered azomethine ylides.
@en
P2093
P304
P356
10.1021/JO005686S
P407
P577
2001-02-01T00:00:00Z