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1. Modern methods in stereoselective aldol reactions
by Mahrwald, Rainer, 1950
2013, 1. Aufl., ISBN 9783527656738, xiv, 536
Aldehydes | Aldol condensation
Book
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2. Full Text Exploring “Through‐Bond” Proximity between the Ion Tag and Reaction Site of an Imidazolium‐Proline Catalyst for the Direct Asymmetric Aldol Reaction
by Bhati, Meeta and Upadhyay, Shruti and Easwar, Srinivasan
European journal of organic chemistry, ISSN 1434-193X, 04/2017, Volume 2017, Issue 13, pp. 1788 - 1793
Water chemistry | Catalyst recycling | Asymmetric catalysis | Ion tags | Aldol reactions | Proline | Analysis
Journal Article
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3. Full Text Towards click chemistry: Multicomponent reactions via combinations of name reactions
by Heravi, Majid M and Zadsirjan, Vahideh and Dehghani, Mahzad and Ahmadi, Tahereh
Tetrahedron, ISSN 0040-4020, 07/2018, Volume 74, Issue 27, pp. 3391 - 3457
Heterocycles | Multicomponent reaction | Ugi reaction | Heck reaction | Aldol reaction | Huisgen reaction | Name reaction | Mannich reaction | Click chemistry | Knoevenagel reaction | Diels-Alder reaction | Michael reaction | Suzuki reaction | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
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4. Full Text Direct Acetophenone–Acetophenone Crossed Aldol Reaction and Aldol Self‐Reaction Promoted by a Tethered Ru–S Complex
by Pommerening, Phillip and Stahl, Timo and Oestreich, Martin
European journal of organic chemistry, ISSN 1434-193X, 05/2018, Volume 2018, Issue 19, pp. 2290 - 2293
Si–H bond activation | Ruthenium | Cooperativity | Aldol reactions | C–C bond formation | Acetophenone | Boron | Ketones | Aldehydes | Dehydrogenation | Reagents
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5. Full Text Chalcogenide–Lewis Acid Mediated Tandem Michael Aldol Reaction — an Alternative to the Morita–Baylis–Hillman Reaction and a New Development
by Kataoka, Tadashi and Kinoshita, Hironori
01/2005, Volume 2005, Issue 1, 14
Michael addition | C–C coupling | Chalcogens | Alkenes | Aldol reactions | C-C coupling | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
Book Review
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6. 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
Journal Article
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7. Full Text Chiral Allenes via Alkynylogous Mukaiyama Aldol Reaction
by Tap, Aurélien and Blond, Aurélie and Wakchaure, Vijay N and List, Benjamin
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2016, Volume 55, Issue 31, pp. 8962 - 8965
organocatalysis | Lewis acids | allenes | aldol reactions | disulfonimides | Enantiomers | Catalysis
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8. Full Text Direct anti Glycolate Aldol Reaction of Protected Chiral N‐Hydroxyacetyl Thiazolidinethiones with Acetals Catalyzed by a Nickel(II) Complex
by Romo, Juan Manuel and Romea, Pedro and Urpí, Fèlix
European journal of organic chemistry, ISSN 1434-193X, 09/2019, Volume 2019, Issue 36, pp. 6296 - 6305
Synthetic methods | Chiral auxiliaries | Aldol reactions | Homogeneous catalysis | Diastereoselectivity | Nickel | Aldehydes | Acetals | Adducts | Organic synthesis | Quiralitat | Síntesi orgànica | Catàlisi homogènia | Chirality
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9. Full Text Total synthesis of (+)-methynolide using a Ti-mediated aldol reaction of a lactyl-bearing oxazolidin-2-one, and a vinylogous Mukaiyama aldol reaction
by Suzuki, Takahiro and Fujimura, Masataka and Fujita, Kazuhiro and Kobayashi, Susumu
Tetrahedron, ISSN 0040-4020, 06/2017, Volume 73, Issue 26, pp. 3652 - 3659
Natural product | Aldol reaction | Oxazolidin-2-one | Convergent synthesis | Total synthesis | Synthesis | Organic compounds
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10. Full Text “Side‐Product Catalysis”: Substrate Autoxidation as an Overlooked Side Reaction Generating a Co‐Catalyst for Enhancing Asymmetric Aldol Reactions
by Heidlindemann, Marcel and Berkessel, Albrecht and Gröger, Harald
ChemCatChem, ISSN 1867-3880, 04/2017, Volume 9, Issue 8, pp. 1383 - 1388
organocatalysis | aldol reaction | asymmetric catalysis | autoxidation | acid co-catalysis | Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology | Aldehydes | Catalysis
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