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chemistry (20) 20
aldol-type reaction (14) 14
physical sciences (13) 13
science & technology (13) 13
organic chemistry (10) 10
catalysis (9) 9
exact sciences and technology (9) 9
aldehydes (8) 8
aldol-type condensation (6) 6
preparations and properties (6) 6
aldol type condensation (4) 4
aldol-type coupling (4) 4
aldol-type reactions (4) 4
diels-alder reaction (4) 4
heterocyclic compounds (4) 4
molecular structure (4) 4
silylformylation (4) 4
synthesis (4) 4
tetrahedrons (4) 4
開発 (4) 4
aldehyd (3) 3
aldol type coupling (3) 3
aldol-type cyclization (3) 3
aldol‐type reactions (3) 3
chemistry, multidisciplinary (3) 3
chemistry, organic (3) 3
heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives (3) 3
indium (3) 3
rhodium catalyst (3) 3
technology (3) 3
反応 (3) 3
合成 (3) 3
3-chromones (2) 2
3-formylchromones (2) 2
aldol type reaction (2) 2
aldol-condensation (2) 2
aldol-type of group-transfer polymerization (2) 2
aldolkondensation (2) 2
aldol‐type of group‐transfer polymerization (2) 2
allylation reactions (2) 2
allylic substitution (2) 2
aluminum selenolates (2) 2
aluminum thiolates (2) 2
analysis (2) 2
aniline (2) 2
aox removal (2) 2
asymmetric aldol reaction (2) 2
asymmetric reaction (2) 2
biological and medical sciences (2) 2
biszinc-tartrate complex (2) 2
carbon-carbon bond formation (2) 2
carbonyls (2) 2
catalysts (2) 2
chiral auxiliary (2) 2
condensed benzenic and aromatic compounds (2) 2
cyclization (2) 2
cyclocarbonylation (2) 2
derivatives (2) 2
diazo compounds (2) 2
diselenoic acid esters (2) 2
electron-deficient dienes (2) 2
elimination reaction (2) 2
engineering (2) 2
engineering, chemical (2) 2
epoxide opening (2) 2
esters (2) 2
ethyl diazoacetate (2) 2
formaldehyde (2) 2
formation of lactams (2) 2
formation of lactones (2) 2
fundamental and applied biological sciences. psychology (2) 2
furans (2) 2
gtp (2) 2
hemiselenothioacetals (2) 2
humans (2) 2
lewis acid catalyst (2) 2
lewis-säure (2) 2
life sciences & biomedicine (2) 2
metal eneselenolates (2) 2
metalle (2) 2
methanol (2) 2
models, molecular (2) 2
noncondensed benzenic compounds (2) 2
oxidative addition of hydrosilane (2) 2
physical chemistry (2) 2
polymer science (2) 2
reductive aldol-type reaction (2) 2
reductive cyclization (2) 2
rhcl3 (2) 2
schiff bases (2) 2
seleno-claisen rearrangement (2) 2
selenothioic acid s-esters (2) 2
sequential chemical reactions (2) 2
silylative bicyclocarbonylation (2) 2
stereoisomerism (2) 2
strategy (2) 2
trapping (2) 2
vinyl selenides (2) 2
ylidenemalononitriles (2) 2
オキサ (2) 2
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1. Full Text Efficient one-pot synthesis of benzopyranobenzopyrans and naphthopyranobenzopyrans by domino aldol-type reaction/hetero Diels–Alder reaction of resorcinols and naphthols
by Lee, Yong Rok and Kim, Yun Mi and Kim, Sung Hong
Tetrahedron, ISSN 0040-4020, 2009, Volume 65, Issue 1, pp. 101 - 108
Hetero Diels–Alder reaction | Aldol-type reaction | Resorcinols | Naphthols | Benzopyranobenzopyrans | Naphthopyranobenzopyrans | Hetero Diels-Alder reaction | Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives | Organic chemistry | Chemistry | Heterocyclic compounds | Exact sciences and technology | Condensed benzenic and aromatic compounds | Preparations and properties | Noncondensed benzenic compounds | Furans | Diels-Alder reaction | Analysis | Ethylenediamines
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2. Full Text Catalytic Enantioselective Aldol‐Type Reaction Using α‐Fluorinated Enolates
by Gong, Yi and Yu, Jin‐Sheng and Hao, Yong‐Jia and Zhou, Ying and Zhou, Jian
Asian journal of organic chemistry, ISSN 2193-5807, 05/2019, Volume 8, Issue 5, pp. 610 - 626
aldol-type reaction | organocatalysis | Catalytic asymmetric | metal catalysis | α-fluorinated enolate precursors | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology | Carbonyl compounds | Carbonyl groups | Optical activity | Alcohol | Catalysis | Enantiomers | Aldehydes | Fluorination | Alcohols | Carbonyls
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3. Full Text Synthesis of novel chromeno-annulated cis-fused pyrano[3,4-c]benzopyran and naphtho pyran derivatives via domino aldol-type/hetero Diels–Alder reaction and their cytotoxicity evaluation
by Madda, Jyothi and Venkatesham, Akkaladevi and Naveen Kumar, Bejjanki and Nagaiah, Kommu and Sujitha, Pombala and Ganesh Kumar, C and Rao, Tadikamalla Prabhakar and Jagadeesh Babu, Nanubolu
Bioorganic & medicinal chemistry letters, ISSN 0960-894X, 09/2014, Volume 24, Issue 18, pp. 4428 - 4434
Aldol-type/hetero Diels–Alder reaction cytotoxicity evaluation | MCF-7 (breast) | Chromeno pyrano[3,4-c]benzopyran and naphtho pyrans | HeLa (cervical) | MDA-MB-231 (breast) | A549 (lung) | Aldol-type/hetero Diels-Alder reaction cytotoxicity evaluation | Chromeno pyrano[3,4-c]benzopyran and | naphtho pyrans | cytotoxicity evaluation | Aldol-type/hetero Diels-Alder reaction | Pyrans - chemical synthesis | Stereoisomerism | Antineoplastic Agents - chemical synthesis | Humans | Naphthols - pharmacology | Models, Molecular | Naphthols - chemistry | Structure-Activity Relationship | Antineoplastic Agents - chemistry | Benzopyrans - chemistry | Dose-Response Relationship, Drug | Benzopyrans - chemical synthesis | MCF-7 Cells | Pyrans - chemistry | HEK293 Cells | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Molecular Structure | HeLa Cells | Benzopyrans - pharmacology | Pyrans - pharmacology | Drug Screening Assays, Antitumor | Naphthols - chemical synthesis | Furans | Resveratrol | Diels-Alder reaction | Index Medicus
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4. Full Text KF/Nano-clinoptilolite Catalyzed Aldol-Type Reaction of Aldehydes with Ethyl Diazoacetate
by Balou, Javad and Khalilzadeh, Mohammad A and Zareyee, Dariush
Catalysis letters, ISSN 1011-372X, 10/2017, Volume 147, Issue 10, pp. 2612 - 2618
Chemistry | KF/nano-clinoptilolite | Aldol-type reaction | Physical Chemistry | Organometallic Chemistry | α-Diazo carbonyl derivatives | Catalysis | Industrial Chemistry/Chemical Engineering | Ethyl diazoacetate | Diazo compounds | Biological products | Fluorides | Catalysts | Aldehydes | Potassium fluoride | Carbonyls
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5. Full Text Cu(I)-catalyzed decarboxylative aldol-type and Mannich-type reactions for asymmetric construction of contiguous trisubstituted and quaternary stereocenters
by Yin, Liang and Kanai, Motomu and Shibasaki, Masakatsu
Tetrahedron, ISSN 0040-4020, 04/2012, Volume 68, Issue 17, pp. 3497 - 3506
Mannich-type reaction | Quaternary stereocenters | Aldol-type reaction | Decarboxylation | Cu(I) catalyst | Hydrolysis | Schiff bases | Nitriles | Aldehydes | Asymmetry | Imines | Racemization | Derivatives | Nucleophiles | Aliphatic compounds
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6. Full Text Efficient synthesis of α-aryl serine derivatives via three-component reactions of aryldiazoacetates, anilines and formaldehyde
by Wang, Chengjin and Liu, Shunying and Xing, Dong and Wang, Xin and Wu, Xiang and Hu, Wenhao
Tetrahedron, ISSN 0040-4020, 12/2013, Volume 69, Issue 52, pp. 11203 - 11208
Three-component reaction | α-Aryl serine derivatives | Aldol-type reaction | Ammonium ylide | Formaldehyde | Trapping | Synthesis | Aniline | Tetrahedrons | Strategy | Derivatives
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7. Full Text Asymmetric Reductive Aldol-Type Reaction with Carbonyl Compounds Using Dialkyl Tartrate as a Chiral Ligand
by Isoda, Motoyuki and Sato, Kazuyuki and Tokura, Yoriko and Tarui, Atsushi and Omote, Masaaki and Ando, Akira
Chemical & pharmaceutical bulletin, ISSN 0009-2363, 2014, Volume 62, Issue 10, pp. 956 - 961
reductive aldol-type reaction | aldol-type cyclization | biszinc–tartrate complex | asymmetric reaction | RhCl(PPh3)3 | Aldol-type cyclization | Biszinc-tartrate complex | Reductive aldol-type reaction | Asymmetric reaction | Cyclization | Stereoisomerism | Ketones - chemistry | Esters | Ligands | Catalysis | Tartrates - chemistry | Zinc - chemistry | Coordination Complexes - chemistry | Rhodium - chemistry | Aldehydes - chemistry | Index Medicus
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8. Full Text Synthesis of electron-deficient dienes bearing a chromonyl moiety via the reaction of 3-formylchromones with ylidenemalononitriles and ethyl α-cyano-β-methylcinnamate
by Korotaev, Vladislav Yu and Barkov, Alexey Yu and Kutyashev, Igor B and Safrygin, Alexander V and Sosnovskikh, Vyacheslav Ya
Tetrahedron, ISSN 0040-4020, 06/2014, Volume 70, Issue 22, pp. 3584 - 3589
Electron-deficient dienes | 3-(Buta-1,3-dienyl)chromones | Ylidenemalononitriles | Aldol type condensation | 3-Formylchromones | Synthesis (chemistry) | Crystallization | Triethylamine | Tetrahedrons | Dichloromethane | Dienes | Bearing
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9. Full Text Toward the synthesis of γ-pyrone-containing natural products: diastereoselective aldol-type reaction of a γ-pyrone
by Takemura, Takuma and Hayakawa, Ichiro and Fukasawa, Emi and Sengoku, Tetsuya and Kigoshi, Hideo
Tetrahedron, ISSN 0040-4020, 08/2012, Volume 68, Issue 32, pp. 6477 - 6484
Diastereoselective aldol-type reaction of a γ-pyrone | Mukaiyama aldol-type reaction of a γ-pyrone | anti-Aldol selectivity | Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives | Organic chemistry | Chemistry | Heterocyclic compounds | Preparations and properties | Exact sciences and technology
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10. Full Text Asymmetric Reductive Aldol-Type Reaction with Carbonyl Compounds Using Dialkyl Tartrate as a Chiral Ligand
by Motoyuki Isoda and Kazuyuki Sato and Yoriko Tokura and Atsushi Tarui and Masaaki Omote and Akira Ando and Faculty of Pharmaceutical Sciences and Setsunan University
Chemical & pharmaceutical bulletin, ISSN 0009-2363, 2014, Volume 62, Issue 10, pp. 956 - 961
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11. Full Text Aldol-type reaction of a 4-pyrone: a straightforward approach to 4-pyrone-containing natural products
by Sengoku, Tetsuya and Takemura, Takuma and Fukasawa, Emi and Hayakawa, Ichiro and Kigoshi, Hideo
Tetrahedron letters, ISSN 0040-4039, 2009, Volume 50, Issue 3, pp. 325 - 328
Aldol-type reaction | Counter cation | 4-Pyrone-containing natural product
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12. Full Text Synthesis of electron-deficient dienes bearing a chromonyl moiety via the reaction of 3-formylchromones with ylidenemalononitriles and ethyl α-cyano-β-methylcinnamate Dedicated to Professor Oleg N. Chupakhin on his 80th birthday
by Korotaev, Vladislav Yu and Barkov, Alexey Yu and Kutyashev, Igor B and Safrygin, Alexander V and Sosnovskikh, Vyacheslav Ya
Tetrahedron, ISSN 0040-4020, 06/2014, Volume 70, Issue 22, pp. 3584 - 3589
Electron-deficient dienes | Aldol type condensation | 3-(Buta-1,3-dienyl)chromones | Ylidenemalononitriles | 3-Formylchromones
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13. Full Text Synthesis of α-diazo-β-hydroxyesters through a one-pot protocol by phase-transfer catalysis: application to enantioselective aldol-type reaction and diastereoselective synthesis of α-amino-β-hydroxyester derivatives
by Hasegawa, Kazuya and Arai, Shigeru and Nishida, Atsushi
Tetrahedron, ISSN 0040-4020, 2006, Volume 62, Issue 7, pp. 1390 - 1401
Aldol-type reaction | α-Diazo-β-hydroxyester | α-Amino-β-hydroxyester | α-Amino-β- hydroxyester
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14. Full Text A novel 3D pillar-layered metal-organic framework: Pore-size-dependent catalytic activity and CO2/N2 affinity
by Ghasempour, Hosein and Azhdari Tehrani, Alireza and Morsali, Ali and Wang, Jun and Junk, Peter C
Polyhedron, ISSN 0277-5387, 04/2020, Volume 180, p. 114422
X-ray crystallography | Coordination polymers, Metal organic Frameworks | Catalysis | Aldol-type reaction | Functional materials
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15. Full Text Indium(I) bromide-promoted stereoselective preparation of cyclopropanes via sequential aldol-type coupling/elimination/Michael-induced ring closure reaction from α,α-dichloroacetophenone and aldehydes
by Peppe, Clovis and das Chagas, Rafael Pavão and Burrow, Robert Alan
Journal of organometallic chemistry, ISSN 0022-328X, 2008, Volume 693, Issue 21, pp. 3441 - 3445
Aldol-type coupling | Sequential chemical reactions | Indium(I) | Elimination reaction | Michael-induced ring closure reaction
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16. Full Text An expedient domino three-component [3+2]-cycloaddition/annulation protocol: regio- and stereoselective assembly of novel polycyclic hybrid heterocycles with five contiguous stereocentres
by Uma Maheswari, Shanmugavel and Perumal, Subbu
Tetrahedron letters, ISSN 0040-4039, 12/2013, Volume 54, Issue 51, pp. 7044 - 7048
Intramolecular aldol-type reactions | 1,3-Dipolar cycloaddition | 2-[Arylmethylidene]-3,4-dihydro-1(2H)-acridinones | Domino reactions | Azomethine ylide | 2-[Arylmethylidene]-3,4-dihydro- 1(2H)-acridinones | Organic chemistry | Cycloaddition | Synthesis | Tetrahedrons | Chemical reactions | Strategy | Transformations | Assembly
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17. Full Text Synthetic Study on Telomerase Inhibitor, D8646-2-6: Synthesis of the Key Intermediate Using Sn(OTf)2 or Sc(OTf)3 Mediated Aldol-Type Reaction and Stille Coupling
by Kanai, Akira and Takeda, Yoshifumi and Kuramochi, Kouji and Nakazaki, Atsuo and Kobayashi, Susumu and Tokyo University of Science (RIKADAI and Faculty of Science and Technology and aFaculty of Pharmaceutical Sciences and bDepartment of Applied Biological Science
Chemical & pharmaceutical bulletin, ISSN 0009-2363, 2007, Volume 55, Issue 3, pp. 495 - 499
aldol-type reaction | scandium triflate | vinyl stannane which contains phosphonate | carbohydrate-containing pyrone | tin triflate | stille coupling | Vinyl stannane which contains phosphonate | Stille coupling | Aldol-type reaction | Scandium triflate | Carbohydrate-containing pyrone | Tin triflate | Scandium - chemistry | Glycosides - chemical synthesis | Molecular Structure | Catalysis | Telomerase - antagonists & inhibitors | Tin Compounds - chemistry | Enzyme Inhibitors - chemical synthesis | Index Medicus
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18. Full Text Enantioselective Aldol-Type Reaction Using Diketene
by Kawase, Takahiro and Takizawa, Shinobu and Jayaprakash, Doss and Sasai, Hiroaki
Synthetic communications, ISSN 0039-7911, 01/2004, Volume 34, Issue 24, pp. 4487 - 4492
Titanium-BINOL complexes | Enantioselective | Aldol-type reaction | Diketene | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
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19. Full Text Enantiocontrolled synthesis of the epoxycyclohexenone moieties of scyphostatin, a potent and specific inhibitor of neutral sphingomyelinase
by Katoh, Tadashi and Izuhara, Takashi and Yokota, Wakako and Inoue, Munenori and Watanabe, Kazuhiro and Nobeyama, Ayaka and Suzuki, Takeyuki
Tetrahedron, ISSN 0040-4020, 2006, Volume 62, Issue 7, pp. 1590 - 1608
Sphingomyelinase | Aldol-type coupling | Diels–Alder reaction | Diels-Alder reaction | Aldehydes
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20. Full Text An electrophilic reaction on tris(2,4-pentanedionato)cobalt in Lewis acidic conditions
by Noguchi, Takatoshi and Fujii, Yuki and Nakano, Yoshiharu
Inorganica Chimica Acta, ISSN 0020-1693, 2006, Volume 359, Issue 7, pp. 2268 - 2270
Pseudoaromaticity | Co(acac) 3 | Aldol type reaction | BF 3–acetic acid complex | Co(acac) | acetic acid complex | Physical Sciences | Chemistry, Inorganic & Nuclear | Chemistry | Science & Technology
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