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Chiral tertiary 2-furyl alcohols: diversified key intermediates to bioactive compounds. Their enantioselective synthesis via (2-furyl)aluminium addition to ketones catalyzed by a titanium catalyst of (S)-BINOL

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-3773(20010316)40:6<1058::aid-anie10580>3.0.co;2-3openalex-snapshot

Enantioselective Synthesis of the Ricciocarpins A and B

inferredcites →https://doi.org/10.1002/1521-3773(20010417)40:8<1488::aid-anie1488>3.0.co;2-bopenalex-snapshot

Application of a Planar Chiralη5-Cyclopentadienylrhenium(I)tricarbonyl Complex in Asymmetric Catalysis: Highly Enantioselective Phenyl Transfer to Aldehydes

inferredcites →https://doi.org/10.1002/1521-3773(20020118)41:2<230::aid-anie230>3.0.co;2-lopenalex-snapshot

Glycosamino Acids: Building Blocks for Combinatorial Synthesis—Implications for Drug Discovery

inferredcites →https://doi.org/10.1002/1521-3773(20021004)41:19<3677::aid-anie3677>3.0.co;2-yopenalex-snapshot

Generation of Libraries of Pharmacophoric Structures with Increased Complexity and Diversity by Employing Polymorphic Scaffolds

inferredcites →https://doi.org/10.1002/anie.199304771openalex-snapshot

Poly(hydroxyalkanoates): A Fifth Class of Physiologically Important Organic Biopolymers?

inferredcites →https://doi.org/10.1002/anie.200301696openalex-snapshot

Chiral Tertiary Alcohols Made By Catalytic Enantioselective Addition of Unreactive Zinc Reagents to Poorly Electrophilic Ketones?

inferredcites →https://doi.org/10.1002/anie.200353129openalex-snapshot

Synthesis of the Furanosteroidal Antibiotic Viridin

inferredcites →https://doi.org/10.1002/anie.200461668openalex-snapshot

Developments in Furan Syntheses

inferredcites →https://doi.org/10.1002/anie.200500469openalex-snapshot

Highly Enantioselective Synthesis of γ‐Hydroxy‐α,β‐acetylenic Esters by Asymmetric Alkyne Addition to Aldehydes

inferredcites →https://doi.org/10.1002/anie.200501511openalex-snapshot

A General Sultone Route to the Pamamycin Macrodiolides—Total Synthesis of Pamamycin‐621A and Pamamycin‐635B

inferredcites →https://doi.org/10.1002/anie.200701201openalex-snapshot

Highly Enantioselective Aryl Additions of [AlAr3(thf)] to Ketones Catalyzed by a Titanium(IV) Catalyst of (S)‐Binol

inferredcites →https://doi.org/10.1002/chem.200501048openalex-snapshot

Highly Enantioselective Addition of In Situ Prepared Arylzinc to Aldehydes Catalyzed by a Series of Atropisomeric Binaphthyl‐Derived Amino Alcohols

inferredcites →https://doi.org/10.1002/chem.200501397openalex-snapshot

trans‐1‐Sulfonylamino‐2‐isoborneolsulfonylaminocyclohexane Derivatives: Excellent Chiral Ligands for the Catalytic Enantioselective Addition of Organozinc Reagents to Ketones

inferredcites →https://doi.org/10.1016/j.tet.2003.10.042openalex-snapshot

Asymmetric alkynylzinc additions to aldehydes and ketones

inferredcites →https://doi.org/10.1016/s0960-894x(02)00197-xopenalex-snapshot

Novel bicyclic oxazolone derivatives as anti-Angiogenic agents

inferredcites →https://doi.org/10.1016/s0968-0896(03)00295-5openalex-snapshot

Synthesis of furanone-Based natural product analogues with quorum sensing antagonist activity

inferredcites →https://doi.org/10.1021/ar000194nopenalex-snapshot

Masked o-Benzoquinones in Organic Synthesis

inferredcites →https://doi.org/10.1021/cr000411yopenalex-snapshot

Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds

inferredcites →https://doi.org/10.1021/cr020050hopenalex-snapshot

Catalytic Enantioselective Addition of Allylic Organometallic Reagents to Aldehydes and Ketones

inferredcites →https://doi.org/10.1021/cr040079gopenalex-snapshot

BINOL: A Versatile Chiral Reagent

inferredcites →https://doi.org/10.1021/ja011242hopenalex-snapshot

Synthesis and Absolute Stereochemistry of Roseophilin

inferredcites →https://doi.org/10.1021/ja020338oopenalex-snapshot

Bis((( S )-binaphthoxy)(isopropoxy)titanium) Oxide as a μ-Oxo-Type Chiral Lewis Acid: Application to Catalytic Asymmetric Allylation of Aldehydes

inferredcites →https://doi.org/10.1021/ja026568kopenalex-snapshot

A Practical Catalytic Asymmetric Addition of Alkyl Groups to Ketones

inferredcites →https://doi.org/10.1021/ja027271popenalex-snapshot

A General, Highly Enantioselective Method for the Synthesis of d and l α-Amino Acids and Allylic Amines

inferredcites →https://doi.org/10.1021/ja0375582openalex-snapshot

Regioselective Synthesis of Unsymmetrical C -Aryl Glycosides Using Silicon Tethers as Disposable Linkers

inferredcites →https://doi.org/10.1021/ja042375gopenalex-snapshot

Biomimetic Synthesis and Structure Elucidation of Rubicordifolin, a Cytotoxic Natural Product from Rubia cordifolia

inferredcites →https://doi.org/10.1021/ja0425740openalex-snapshot

Catalytic Asymmetric Vinylation and Dienylation of Ketones

inferredcites →https://doi.org/10.1021/ja054871qopenalex-snapshot

Dinuclear Zn-Catalyzed Asymmetric Alkynylation of Unsaturated Aldehydes

inferredcites →https://doi.org/10.1021/ja058454popenalex-snapshot

Catalytic Enantioselective Nozaki−Hiyama Allylation Reaction with Tethered Bis(8-quinolinolato) (TBOx) Chromium Complex

inferredcites →https://doi.org/10.1021/ja062080yopenalex-snapshot

Remarkably Efficient Enantioselective Titanium(IV)−(R)-H8-BINOLate Catalyst for Arylations to Aldehydes by Triaryl(tetrahydrofuran)aluminum Reagents

inferredcites →https://doi.org/10.1021/ja067083popenalex-snapshot

Total Synthesis of Abyssomicin C, Atrop-abyssomicin C, and Abyssomicin D: Implications for Natural Origins of Atrop-abyssomicin C

inferredcites →https://doi.org/10.1021/ja068047topenalex-snapshot

Total Synthesis of (+)-Nakadomarin A

inferredcites →https://doi.org/10.1021/ja068150iopenalex-snapshot

Total Synthesis of (±)-Merrilactone A via Catalytic Nazarov Cyclization

inferredcites →https://doi.org/10.1021/ja973169uopenalex-snapshot

Catalytic Asymmetric Addition of ZnPh2 to Ketones: Enantioselective Formation of Quaternary Stereocenters

inferredcites →https://doi.org/10.1021/ja973559gopenalex-snapshot

An Enantioselective Construction of the ABC System of Taxol

inferredcites →https://doi.org/10.1021/jo050957qopenalex-snapshot

Synthesis of 2,3-Di- and 2,3,4-Trisubstituted Furans from 1,2-Dioxines Generated by an Enyne-RCM/Diels−Alder Reaction Sequence

inferredcites →https://doi.org/10.1021/ol034278iopenalex-snapshot

Highly Diastereoselective and Asymmetric Diels−Alder Reactions of Masked o-Benzoquinones with Chiral Racemic and Homochiral Furans. Synthesis of Optically Active Tricyclic γ-Lactones

inferredcites →https://doi.org/10.1039/b600091fopenalex-snapshot

Catalytic asymmetric approaches towards enantiomerically enriched diarylmethanols and diarylmethylamines

inferredcites →https://doi.org/10.1039/b602596jopenalex-snapshot

Syntheses of polysubstituted furans: recent developments

inferredcites →https://doi.org/10.1039/b617746hopenalex-snapshot

Asymmetric catalysis for the construction of quaternary carbon centres: nucleophilic addition on ketones and ketimines

inferredcites →https://doi.org/10.1039/b707703copenalex-snapshot

AlAr3(THF): highly efficient reagents for cross-couplings with aryl bromides and chlorides catalyzed by the economic palladium complex of PCy3

inferredcites →https://doi.org/10.1039/p19900003214openalex-snapshot

Enantioselective furylation of prochiral aldehydes by difurylzinc in the presence of a chiral amino alcohol: asymmetric synthesis of 2-furylmethanols

inferredcites →https://doi.org/10.1081/car-200049688openalex-snapshot

Synthesis of Acetylated Ranunculin Diastereoisomers and δ–Glucosyloxy–γ–Oxo Esters from α or β Glucosylmethylfurfural

inferredcites →https://doi.org/10.1139/v02-105openalex-snapshot

Exploratory synthetic investigations related to 12a-deoxypillaromycinone

inferredcites →https://doi.org/10.1351/pac200577010139openalex-snapshot

Use of furans in synthesis of bioactive compounds

inferredcites →https://doi.org/10.2174/1385272053369222openalex-snapshot

Photooxygenation of Heterocycles

inferredcites →https://doi.org/10.2174/138527206778249847openalex-snapshot

Asymmetric Addition to Ketones: Enantioselective Formation of Tertiary Alcohols

inferredcites →https://doi.org/10.3987/com-00-s(i)53openalex-snapshot

Diastereoselective Addition of Organometallic Reagents to (R)-2,3-Isopropylidenedioxy-1-(2-furyl)-1-propanone Yielding Chiral Tertiary Furyl Carbinols

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4651063openalex-extracted

Copper-Assisted Palladium Catalyzed the Cross-Coupling Reaction of Alknylalane Reagents with 2-Thiobenzo[D]Thiazoles Via C-S Bond Cleavage

inferred← citeshttps://doi.org/10.1002/9780470682531.pat0833openalex-snapshot

Organoaluminum Compounds in Catalytic Enantioselective C C Bond Forming Reactions

inferred← citeshttps://doi.org/10.1002/adsc.201000311openalex-snapshot

Extremely Efficient Cross‐Coupling of Benzylic Halides with Aryltitanium Tris(isopropoxide) Catalyzed by Low Loadings of a Simple Palladium(II) Acetate/Tris(p‐tolyl)phosphine System

inferred← citeshttps://doi.org/10.1002/adsc.201200672openalex-snapshot

Enantioselective Additions of Aryltitanium Tris(isopropoxide) to Ketones: Structure of [(i‐PrO)2Ti{μ‐(S)‐BINOLate}(μ‐O‐i‐Pr)TiPh(O‐i‐Pr)2], Study of Mechanistic and Stereochemical Insights

inferred← citeshttps://doi.org/10.1002/ange.201005124openalex-snapshot

Quaternary Carbon Stereogenic Centers through Copper‐Catalyzed Enantioselective Allylic Substitutions with Readily Accessible Aryl‐ or Heteroaryllithium Reagents and Aluminum Chlorides

inferred← citeshttps://doi.org/10.1002/ange.201204579openalex-snapshot

Katalytische asymmetrische Synthese von Allylalkoholen und Allylalkohol‐Derivaten und deren Anwendung in der organischen Synthese

inferred← citeshttps://doi.org/10.1002/anie.201005124openalex-snapshot

Quaternary Carbon Stereogenic Centers through Copper‐Catalyzed Enantioselective Allylic Substitutions with Readily Accessible Aryl‐ or Heteroaryllithium Reagents and Aluminum Chlorides

inferred← citeshttps://doi.org/10.1002/anie.201204579openalex-snapshot

Catalytic Asymmetric Synthesis of Allylic Alcohols and Derivatives and their Applications in Organic Synthesis

inferred← citeshttps://doi.org/10.1002/cctc.201300655openalex-snapshot

Catalytic Asymmetric Arylation of Enals to Enantioenriched Linear Trisubstituted Allylic Secondary Alcohols by using Aryl Lithiums Generated In Situ from Aryl Bromides

inferred← citeshttps://doi.org/10.1002/chem.201203946openalex-snapshot

Practical Enantioselective Arylation and Heteroarylation of Aldehydes with In Situ Prepared Organotitanium Reagents Catalyzed by 3‐Aryl‐H8‐BINOL‐Derived Titanium Complexes

inferred← citeshttps://doi.org/10.1002/chem.201303061openalex-snapshot

Improved Synthesis of Cyclic Tertiary Allylic Alcohols by Asymmetric 1,2‐Addition of AlMe3 to Enones

inferred← citeshttps://doi.org/10.1002/chem.201601854openalex-snapshot

Enhancement of the Catalytic Activity of Chiral H8‐BINOL Titanium Complexes by Introduction of Sterically Demanding Groups at the 3‐Position

inferred← citeshttps://doi.org/10.1002/chem.201701395openalex-snapshot

Catalytic Enantioselective Arylation and Heteroarylation of Ketones with Organotitanium Reagents Generated In Situ

inferred← citeshttps://doi.org/10.1002/chin.200838096openalex-snapshot

ChemInform Abstract: Chiral Tertiary 2‐Furyl Alcohols: Diversified Key Intermediates to Bioactive Compounds. Their Enantioselective Synthesis via (2‐Furyl)aluminum Addition to Ketones Catalyzed by a Titanium Catalyst of (S)‐BINOL.

inferred← citeshttps://doi.org/10.1002/chir.21018openalex-snapshot

Room temperature and highly enantioselective additions of alkyltitanium reagents to aldehydes catalyzed by a titanium catalyst of (R)‐h8‐binol

inferred← citeshttps://doi.org/10.1002/cjoc.201180303openalex-snapshot

Synthesis of Novel 1,4‐Bissulfonamide Ligands for Enantioselective Addition of Diethylzinc to Aldehydes

inferred← citeshttps://doi.org/10.1007/3418_2012_39openalex-snapshot

Organoaluminum Couplings to Carbonyls, Imines, and Halides

inferred← citeshttps://doi.org/10.1007/7081_2012_79openalex-snapshot

Furans and Benzofurans

inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00105-1openalex-snapshot

1.03 Organoaluminum Reagents

inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.078openalex-snapshot

Reaction of Grignard reagents with carbonyl compounds under continuous flow conditions

inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.072openalex-snapshot

Palladium-catalyzed coupling reactions of (ArCH2)Ti(O-i-Pr)3 with aromatic or heteroaromatic bromides

inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.001openalex-snapshot

Enantioselective titanium-promoted 1,2-additions of carbon nucleophiles to carbonyl compounds

inferred← citeshttps://doi.org/10.1016/j.tet.2021.132564openalex-snapshot

Cross-coupling reaction of organoalane reagents with 2-mercaptobenzo-5-membered heterocycles for efficient synthesis of benzo-5-membered heterocycle sulfides

inferred← citeshttps://doi.org/10.1016/j.tet.2024.133850openalex-snapshot

Copper-assisted palladium catalyzed the cross-coupling reaction of Alknylalane reagents with 2-Thiobenzo[d]thiazoles via C–S bond cleavage

inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.05.018openalex-snapshot

Synthesis, characterization, and structures of arylaluminum reagents and asymmetric arylation of aldehydes catalyzed by a titanium complex of an N-sulfonylated amino alcohol

inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot

Chapter 5.3 Five-membered ring systems: Furans and benzofurans

inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70034-0openalex-snapshot

Chapter 5.3: Five-Membered Ring Systems: Furans and Benzofurans

inferred← citeshttps://doi.org/10.1021/acs.joc.5b01410openalex-snapshot

Asymmetric Addition of Pyridyl Aluminum Reagents to Aldehydes Catalyzed by a Titanium(IV) Catalytic System of (R)-H8-BINOLate

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03379openalex-snapshot

Asymmetric Direct 1,2-Addition of Aryl Grignard Reagents to Aryl Alkyl Ketones

inferred← citeshttps://doi.org/10.1021/acscatal.0c02805openalex-snapshot

N -(Hetero)arylations with Metalated (Hetero)aryls: Recent Advances in First-Row Transition-Metal-Mediated Cross-Couplings

inferred← citeshttps://doi.org/10.1021/ja9046747openalex-snapshot

Practical Catalytic Asymmetric Synthesis of Diaryl-, Aryl Heteroaryl-, and Diheteroarylmethanols

inferred← citeshttps://doi.org/10.1039/c1cc14206bopenalex-snapshot

Simple and efficient nickel-catalyzed cross-coupling reaction of alkynylalanes with benzylic and aryl bromides

inferred← citeshttps://doi.org/10.1039/c2cc31127eopenalex-snapshot

Enantioselective recognition by a highly ordered porphyrin-assembly on a chiral molecular gel

inferred← citeshttps://doi.org/10.1039/c2ob25303hopenalex-snapshot

An efficient nickel-catalyzed alkenylation of functionalized benzylic halides with alkenylaluminum reagents

inferred← citeshttps://doi.org/10.1039/d3nj02026fopenalex-snapshot

The cross-coupling reaction of organoalane reagents with 2-methylthiobenzo[ d ]thiazoles via C–S bond cleavage catalyzed by nickel

inferred← citeshttps://doi.org/10.1246/bcsj.20090232openalex-snapshot

Catalytic Enantioselective Alkylation and Arylation of Aldehydes by Using Grignard Reagents

inferred← citeshttps://doi.org/10.70675/e743d4abz5b6az450cz8a64zb705408734eaopenalex-snapshot

Allylboration énantiosélective et organocatalysée d’alpha-céto-amides : applications à la synthèse d’un produit naturel et de composés spiraniques

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