About: New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride

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About: New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride Goto Sponge NotDistinct Permalink

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scholarly article by Teruaki Mukaiyama et al published November 1974 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1974 (uk) im November 1974 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Teruaki Mukaiyama et al published November 1974 in Journal of the American Chemical Society (en)
publication date	wds:Q56288441-7F4563D7-EF94-4ADB-B199-C35E7E67127D
publication date	1974-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56288441-05A54D28-982C-4C2D-AF3A-AF030AD06D50
language of work or name	English
author name string	wds:Q56288441-166336D4-637A-4857-B960-AC654E5B7153 wds:Q56288441-2F18E99E-5A5C-4D9C-A81C-5BB964B486EA wds:Q56288441-B327615C-29B1-411D-9E6A-CFD63CA6824D
author name string	Teruaki Mukaiyama Koichi Narasaka Kazuo Banno
rdfs:label	New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride (en) New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride (nl)
skos:prefLabel	New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride (en) New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride (nl)
name	New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride (en) New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride (nl)
title	wds:Q56288441-2F18FA67-3590-4BDC-9F94-24DC2A8655A9
title	New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride (en)
page(s)	wds:Q56288441-50AC4DCC-50F2-482A-B7F2-7FC83B05E2BE
page(s)	7503-7509
instance of	wds:Q56288441-25EBB3C1-FE8A-475D-B440-433D89DBE4AD
instance of	scholarly article
main subject	wds:Q56288441-f3c8cc50-fc67-4e62-80ae-77faad464cf6
main subject	titanium
published in	wds:Q56288441-FB4505FE-9E6B-4F68-A09D-F1DA84A2092C
published in	Journal of the American Chemical Society
issue	wds:Q56288441-65A2978D-A9AE-4862-A338-312DE1D5582A
volume	wds:Q56288441-4E62875D-0326-4C24-A415-4C94C75243DF
issue	24
volume	96
DOI	wds:Q56288441-F079AA1B-066D-470E-8D30-8F762F5607AE
DOI	http://dx.doi.org/10.1021/JA00831A019
DOI	10.1021/JA00831A019
ResearchGate publication ID	wds:Q56288441-BE0F0C75-5BD6-4CF2-8326-6B2C4EE766A0
ResearchGate publication ID	231472328
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56288441
is cites work of	The organocatalytic vinylogous aldol reaction: recent advances Total synthesis of brevetoxin A Substituted hepta-1,6-dien-3-ones with green/fruity odours green/galbanum olfactophore model. Catalytic enantioselective decarboxylative reactions using organocatalysts The chemistry of the polycyclic polyprenylated acylphloroglucinols The first direct and enantioselective cross-aldol reaction of aldehydes Disulfonimide-catalyzed asymmetric vinylogous and bisvinylogous Mukaiyama aldol reactions A new chiral oxathiane: synthesis, resolution and absolute configuration determination by vibrational circular dichroism 4-Phenylbutanoyl-2(S)-acylpyrrolidines and 4-phenylbutanoyl-L-prolyl-2(S)-acylpyrrolidines as prolyl oligopeptidase inhibitors. The Mukaiyama aldol reaction: 40 years of continuous development. Synthesis of the next-generation therapeutic antibodies that combine cell targeting and antibody-catalyzed prodrug activation. Silyl ketene imines: highly versatile nucleophiles for catalytic, asymmetric synthesis Design, synthesis and initial biological evaluation of a novel pladienolide analog scaffold Self-Assembly of Disorazole C1 through a One-Pot Alkyne Metathesis Homodimerization Strategy Rapid and stereochemically flexible synthesis of polypropionates: super-silyl-governed aldol cascades The impact of the Mukaiyama aldol reaction in total synthesis Rh-Catalyzed AldehydeAldehyde Cross-Aldol Reaction under Base-Free Conditions: In Situ Aldehyde-Derived Enolate Formation through Orthogonal Activation Rhodium-Catalyzed Cross-Aldol Reaction: In Situ Aldehyde-Enolate Formation from Allyloxyboranes and Primary Allylic Alcohols Wherefore Art Thou Copper? Structures and Reaction Mechanisms of Organocuprate Clusters in Organic Chemistry Self-Assembly of Disorazole C1 through a One-Pot Alkyne Metathesis Homodimerization Strategy Mukaiyama Aldol Reactions in Aqueous Media Highly enantioselective construction of 3-hydroxy oxindoles through a decarboxylative aldol addition of trifluoromethyl α-fluorinated gem-diols to N-benzyl isatins Syntheses of γ,δ-unsaturated alcohols from allylsilanes and carbonyl compounds in the presence of titanium tetrachloride Total synthesis of the antimitotic marine macrolide (-)-leiodermatolide Substitution reactions of 2-benzenesulphonyl cyclic ethers with carbon nucleophiles Expedient synthesis of unsaturated amide alkaloids from Piper spp: Exploring the scope of recent methodology Enantioselective [4 + 2]-Annulation of Chiral Crotylsilanes: Application to the Synthesis of a C1−C22 Fragment of Leucascandrolide A The Directed Aldol Reaction Lewis acid mediated aldol condensations using thioester silyl ketene acetals Comparison of Cu-ZSM-5 zeolites and Cu-MOF-505 metal-organic frameworks as heterogeneous catalysts for the Mukaiyama aldol reaction: a DFT mechanistic study. The one hundred and fifty year history of the Department of Chemistry, the University of Tokyo. A claisen rearrangement strategy for the three-atom ring expansion of cyclic ketones. A total synthesis of (±) precapnelladiene Challenges and discoveries in the total synthesis of complex polyketide natural products. Synthetic studies toward the brasilinolides: controlled assembly of a protected C1-C38 polyol based on fragment union by complex aldol reactions Rhodium-Catalyzed Cross-Aldol Reaction: In Situ Aldehyde-Enolate Formation from Allyloxyboranes and Primary Allylic Alcohols Distillable ionic liquids for a new multicomponent reaction Amphoteric Character of 2-Vinyloxiranes: Synthetic Equivalents of beta,gamma-Unsaturated Aldehydes and a Vinylogous Enolate We thank Professor Batey and his group for providing the allyl and crotyltrifluoroborates. This work was supported by the Nat Total synthesis of odoamide, a novel cyclic depsipeptide, from an Okinawan marine cyanobacterium. Total Synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 Reveals Non-Identity with the Natural Product. Stereochemical Definition of the Natural Product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 by Total Synthesis and Comparative Analyses. Efficient Mukaiyama aldol reaction in water with TiO4 tetrahedra on a hydrophobic mesoporous silica surface. Asymmetric Aldol Reaction with Formaldehyde: a Challenging Process. Pentafulvene-derived η3-allyltitanocenes as intermediates for the stereoselective functionalization of 5-membered carbocycles Typical Reactions Catalytic Enantioselective Aldol Addition Reactions Novel approach for the introduction of a C-1 oxygenated group on the decalin skeleton: first asymmetric total synthesis of 1S,6S-dihydroxy-eudesm-3-ene
is cites work of	wds:Q28265878-5999FA63-CE1F-4380-BBE5-14B6F6E83251 wds:Q42397583-61E2E617-FD2A-4B34-8004-B3881437DC69 wds:Q31008966-4D9F105B-15B9-4DBB-9951-ED6D7EB8E0F3 wds:Q38165729-40C6AF18-13DF-4377-8EC0-0B53E7346CED wds:Q51036020-A0E9DCFE-24CE-4835-A87E-3FD7A3E21CAE wds:Q61632850-FCA5038A-416B-42A0-8D5A-375FAE9B6F17 wds:Q38124790-9026D1F9-21CD-4596-A810-16A9FBA2FC19 wds:Q42704003-9DCF85CE-2345-42D3-BB4A-364D89E8D699 wds:Q42734627-5E8B89FA-6AA1-4D49-A78D-C4F82128AE1F wds:Q56954360-3DE4F1E9-61E0-4A3F-A83B-C83BADA7A7E1 wds:Q57740726-2105A13F-AA50-49BA-85CB-F39980394028 wds:Q62520744-C47CE166-BA8B-40A5-9E7E-0855F10FA6EA wds:Q54152339-EB7ABE4B-D46F-4C4F-A0F5-F41991C66CFC

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