DABCO-catalyzed 1,4-bromolactonization of conjugated enynes: highly stereoselective formation of a stereogenic center and an axially chiral allene.
about
Preparative and mechanistic studies toward the rational development of catalytic, enantioselective selenoetherification reactionsLewis base catalysis of bromo- and iodolactonization, and cycloetherificationEnantioselective dichlorination of allylic alcohols.A rhodium(I)-oxygen adduct as a selective catalyst for one-pot sequential alkyne dimerization-hydrothiolation tandem reactions.Catalytic, asymmetric halofunctionalization of alkenes--a critical perspective.Allylic and allenic halide synthesis via NbCl(5)- and NbBr(5)-mediated alkoxide rearrangements.Stereoselective Halogenation in Natural Product Synthesis.Dearomatization through Halofunctionalization Reactions.Rhodium-catalyzed chemo- and regioselective cross-dimerization of two terminal alkynes.Dynamic kinetic resolution of biaryl atropisomers via peptide-catalyzed asymmetric bromination.Tetrasubstituted allenes by Pd0-catalyzed three-component tandem Michael addition/cross-coupling reaction.Recent advances in stereoselective bromofunctionalization of alkenes using N-bromoamide reagents.Biomimetic Desymmetrization of a Carboxylic Acid.Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides.Atroposelective organocatalysis
P2860
Q34310326-CABA122A-2BFE-4399-BE1F-98D8952C6FB6Q34375817-58A2BC70-EA5C-47EF-896E-2771863D9646Q35021046-69F6CDFA-8F42-49F7-BDFD-9CF8B36E9D29Q35912629-CEFD2FF8-CD1D-4A73-AC73-200B3D768836Q36485386-668656DC-CB17-4832-AB2A-F5010BF6A374Q37368334-2EFBB5AB-42CB-4608-B9ED-FD9B3E1C3F34Q38718959-F77BACA0-F9B1-4E15-BBAB-483A0860F2E1Q38885664-A8CE4C32-ABAC-40F7-8B63-892B81CA8BF6Q41421834-A876E5E1-80AC-4A5D-8C99-472B16D59EC5Q41833099-EB4D18A5-90C4-43B2-801A-F58C38BB7926Q43189179-A1F5E2BF-5B2B-4D81-B998-EDC0241AFD9BQ43832773-70679BA1-CC68-48FF-84B9-52180D3AE70FQ48106502-AC42EE81-4F6D-4E20-8BE4-8C7C445D49F0Q52797301-94A7B535-4ABD-4EAA-9142-1F112B88D7D7Q56986074-275EB3E5-2B10-4B43-A1FD-5261C97CA45D
P2860
DABCO-catalyzed 1,4-bromolactonization of conjugated enynes: highly stereoselective formation of a stereogenic center and an axially chiral allene.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh-hant
name
DABCO-catalyzed 1,4-bromolacto ...... and an axially chiral allene.
@en
DABCO-catalyzed 1,4-bromolacto ...... and an axially chiral allene.
@nl
type
label
DABCO-catalyzed 1,4-bromolacto ...... and an axially chiral allene.
@en
DABCO-catalyzed 1,4-bromolacto ...... and an axially chiral allene.
@nl
prefLabel
DABCO-catalyzed 1,4-bromolacto ...... and an axially chiral allene.
@en
DABCO-catalyzed 1,4-bromolacto ...... and an axially chiral allene.
@nl
P2093
P356
P1476
DABCO-catalyzed 1,4-bromolacto ...... and an axially chiral allene.
@en
P2093
P304
P356
10.1021/JA8099008
P407
P577
2009-03-01T00:00:00Z