Confinement-Controlled, Either syn- or anti-Selective Catalytic Asymmetric Mukaiyama Aldolizations of Propionaldehyde Enolsilanes
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Confinement-Controlled, Either syn- or anti-Selective Catalytic Asymmetric Mukaiyama Aldolizations of Propionaldehyde Enolsilanes
Authors
Keywords
-
Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 36, Pages 14475-14481
Publisher
American Chemical Society (ACS)
Online
2021-08-27
DOI
10.1021/jacs.1c07447
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Catalytic Asymmetric Synthesis of Unprotected β2-Amino Acids
- (2021) Chendan Zhu et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- The Silicon–Hydrogen Exchange Reaction: A Catalytic σ-Bond Metathesis Approach to the Enantioselective Synthesis of Enol Silanes
- (2020) Hui Zhou et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Catalytic enantiocontrol over a non-classical carbocation
- (2020) Roberta Properzi et al. Nature Chemistry
- Confinement as a Unifying Element in Selective Catalysis
- (2020) Benjamin Mitschke et al. Chem
- Acetaldehyde Silyl Enol Ethers in Enantioselective Mukaiyama Aldol Reactions: Enzyme-Like Organocatalysis in Action
- (2019) Luca Dell'Amico et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- IDPi Catalysis
- (2019) Benjamin List et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- The Catalytic Asymmetric Mukaiyama-Michael Reaction of Silyl Ketene Acetals with α,β-Unsaturated Methyl Esters
- (2018) Tim Gatzenmeier et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Approaching sub-ppm-level asymmetric organocatalysis of a highly challenging and scalable carbon–carbon bond forming reaction
- (2018) Han Yong Bae et al. Nature Chemistry
- Discovery of Presaccharothriolide X, a Retro-Michael Reaction Product of Saccharothriolide B, from the Rare Actinomycete Saccharothrix sp. A1506
- (2018) Shan Lu et al. ORGANIC LETTERS
- Scalable and Highly Diastereo- and Enantioselective Catalytic Diels–Alder Reaction of α,β-Unsaturated Methyl Esters
- (2018) Tim Gatzenmeier et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Confined acids catalyze asymmetric single aldolizations of acetaldehyde enolates
- (2018) Lucas Schreyer et al. SCIENCE
- Difluoromethyl Bioisostere: Examining the “Lipophilic Hydrogen Bond Donor” Concept
- (2017) Yossi Zafrani et al. JOURNAL OF MEDICINAL CHEMISTRY
- CF2H, a Hydrogen Bond Donor
- (2017) Chanan D. Sessler et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Stereodivergence in Asymmetric Catalysis
- (2017) Simon Krautwald et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Total Synthesis of Nannocystin Ax
- (2017) Caroline Poock et al. ORGANIC LETTERS
- Second Generation of Aldol Reaction
- (2016) Wafa Gati et al. ACCOUNTS OF CHEMICAL RESEARCH
- Antarlides: A New Type of Androgen Receptor (AR) Antagonist that Overcomes Resistance to AR-Targeted Therapy
- (2016) Shun Saito et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Extremely Active Organocatalysts Enable a Highly Enantioselective Addition of Allyltrimethylsilane to Aldehydes
- (2016) Philip S. J. Kaib et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Development and Applications of Disulfonimides in Enantioselective Organocatalysis
- (2015) Thomas James et al. CHEMICAL REVIEWS
- Catalytic Asymmetric Iterative/Domino Aldehyde Cross-Aldol Reactions for the Rapid and Flexible Synthesis of 1,3-Polyols
- (2015) Luqing Lin et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Diisopinocampheylborane-Mediated Reductive Aldol Reactions: Highly Enantio- and Diastereoselective Synthesis ofsynAldols fromN-Acryloylmorpholine
- (2013) Philippe Nuhant et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- The Mukaiyama Aldol Reaction: 40 Years of Continuous Development
- (2013) Jun-ichi Matsuo et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- The Impact of the Mukaiyama Aldol Reaction in Total Synthesis
- (2013) S. B. Jennifer Kan et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Rapid and Stereochemically Flexible Synthesis of Polypropionates: Super-Silyl-Governed Aldol Cascades
- (2012) Patrick B. Brady et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Chiral-Anion-Dependent Inversion of Diastereo- and Enantioselectivity in Carbonyl Crotylation via Ruthenium-Catalyzed Butadiene Hydrohydroxyalkylation
- (2012) Emma L. McInturff et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Enantioselective C-H Crotylation of Primary Alcohols via Hydrohydroxyalkylation of Butadiene
- (2012) J. R. Zbieg et al. SCIENCE
- A More Comprehensive and Highly Practical Solution to Enantioselective Aldehyde Crotylation
- (2011) Hyunwoo Kim et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Relevance of Weak Hydrogen Bonds in the Conformation of Organic Compounds and Bioconjugates: Evidence from Recent Experimental Data and High-Levelab InitioMO Calculations
- (2010) Osamu Takahashi et al. CHEMICAL REVIEWS
- A Powerful Chiral Counteranion Motif for Asymmetric Catalysis
- (2009) Pilar García-García et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Redox Economy in Organic Synthesis
- (2009) Noah Z. Burns et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- anti-Diastereo- and Enantioselective Carbonyl Crotylation from the Alcohol or Aldehyde Oxidation Level Employing a Cyclometallated Iridium Catalyst: α-Methyl Allyl Acetate as a Surrogate to Preformed Crotylmetal Reagents
- (2009) In Su Kim et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Synthesis at the molecular frontier
- (2009) Paul A. Wender et al. NATURE
- Design and synthesis of ansamycin antibiotics
- (2008) Iwona E. Wrona et al. COMPTES RENDUS CHIMIE
- Cebulactams A1 and A2, new macrolactams isolated from Saccharopolyspora cebuensis, the first obligate marine strain of the genus Saccharopolyspora
- (2008) Sheila Marie Pimentel-Elardo et al. TETRAHEDRON LETTERS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started