Stereoselective intramolecular [4 + 3] cycloadditions of nitrogen-stabilized chiral oxyallyl cations via epoxidation of N-tethered allenamides.

Stereoselective intramolecular [4 + 3] cycloadditions of nitrogen-stabilized chiral oxyallyl cations via epoxidation of N-tethered allenamides.

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http://www.wikidata.org/entity/Q44617481
Enantioselective synthesis of 2,2,5-tri- and 2,2,5,5-tetrasubstituted tetrahydrofurans via [4 + 2] cycloaddition and ring-opening cross-metathesisAllenamides: a powerful and versatile building block in organic synthesis.Control of regioselectivity and stereoselectivity in (4 + 3) cycloadditions of chiral oxyallyls with unsymmetrically disubstituted furans.Reactions of cyclopropanone acetals with alkyl azides: carbonyl addition versus ring-opening pathwaysSilicon-initiated carbonylative carbotricyclization and [2+2+2+1] cycloaddition of enediynes catalyzed by rhodium complexesThe first transannular [4+3] cycloaddition reaction: synthesis of the ABCD ring structure of cortistatinsStereoselectivities and regioselectivities of (4 + 3) cycloadditions between allenamide-derived chiral oxazolidinone-stabilized oxyallyls and furans: experiment and theory.An approach to cyclohepta[b]indoles through an allenamide (4 + 3) cycloaddition-Grignard cyclization-Chugaev elimination sequence.Synthesis of amido-spiro[2.2]pentanes via Simmons-Smith cyclopropanation of allenamides.Intramolecular oxyallyl-carbonyl (3 + 2) cycloadditions.Regioselectivities of (4 + 3) cycloadditions between furans and oxazolidinone-substituted oxyallyls.Thermal intramolecular [4 + 2] cycloadditions of allenamides: a stereoselective tandem propargyl amide isomerization-cycloaddition.(4+3) cycloaddition reactions of nitrogen-stabilized oxyallyl cations.Developing a diastereoselective intramolecular [4+3] cycloaddition of nitrogen-stabilized oxyallyl cations derived from N-sulfonyl-substituted allenamides.The conversion of allenes to strained three-membered heterocycles.
P2860

Stereoselective intramolecular [4 + 3] cycloadditions of nitrogen-stabilized chiral oxyallyl cations via epoxidation of N-tethered allenamides.

Item
http://www.wikidata.org/entity/Q44617481
description
2003 nî lūn-bûn
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name
Stereoselective intramolecular ...... ion of N-tethered allenamides.
@en
Stereoselective intramolecular ...... ion of N-tethered allenamides.
@nl
type
label
Stereoselective intramolecular ...... ion of N-tethered allenamides.
@en
Stereoselective intramolecular ...... ion of N-tethered allenamides.
@nl
prefLabel
Stereoselective intramolecular ...... ion of N-tethered allenamides.
@en
Stereoselective intramolecular ...... ion of N-tethered allenamides.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P921
P356
P1433
P1476
Stereoselective intramolecular ...... ion of N-tethered allenamides.
@en
P2093
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P921