Stereoselective Synthesis of Tetrahydropyrans through Tandem and Organocatalytic Oxa-Michael Reactions: Synthesis of the Tetrahydropyran Cores of ent-(+)-Sorangicin A
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Stereoselective Synthesis of Tetrahydropyrans through Tandem and Organocatalytic Oxa-Michael Reactions: Synthesis of the Tetrahydropyran Cores of ent-(+)-Sorangicin A
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2012, Issue 5, Pages 1025-1032
Publisher
Wiley
Online
2011-12-27
DOI
10.1002/ejoc.201101549
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- A Stereoselective Formal Synthesis of Leucascandrolide A
- (2011) Kiyoun Lee et al. ORGANIC LETTERS
- Stereoselective Synthesis of 2,6-trans-Tetrahydropyran via Primary Diamine-Catalyzed Oxa-Conjugate Addition Reaction of α,β-Unsaturated Ketone: Total Synthesis of Psymberin
- (2011) Seong Rim Byeon et al. ORGANIC LETTERS
- A Formal Synthesis of SCH 351448
- (2011) Heekwang Park et al. ORGANIC LETTERS
- Formal Synthesis of (+)-Sorangicin A
- (2011) Michael T. Crimmins et al. ORGANIC LETTERS
- Formal total synthesis of the myxobacteria metabolite apicularen A via a transannular oxy-Michael addition
- (2011) Ferdows Hilli et al. TETRAHEDRON
- Indium(III) chloride-catalyzed Mukaiyama–Michael addition: synthesis of 2,6-anti-tetrahydropyrans
- (2011) Sin-Siu Chua et al. TETRAHEDRON
- Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition
- (2011) Duncan Gill et al. TETRAHEDRON
- FeCl3·6H2O-catalyzed synthesis of substituted cis-2,6-tetrahydropyrans from ζ-hydroxy allylic derivatives
- (2011) Amandine Guérinot et al. TETRAHEDRON
- An asymmetric Maitland–Japp reaction: a highly enantioselective synthesis of tetrahydropyran-4-ones
- (2011) Mudassar Iqbal et al. TETRAHEDRON
- A new strategy for the synthesis of substituted dihydropyrones and tetrahydropyrones via palladium-catalyzed coupling of thioesters
- (2011) Haruhiko Fuwa et al. TETRAHEDRON
- Synthesis of Dihydropyran Subunit of (+)-Sorangicin A Using RCM Reaction
- (2010) BULLETIN OF THE KOREAN CHEMICAL SOCIETY
- Iodine-Catalyzed Highly Diastereoselective Synthesis oftrans-2,6-Disubstituted-3,4-Dihydropyrans: Application to Concise Construction of C28-C37 Bicyclic Core of (+)-Sorangicin A
- (2010) Debendra K. Mohapatra et al. CHEMISTRY-A EUROPEAN JOURNAL
- Total Synthesis of Cyanolide A and Confirmation of Its Absolute Configuration
- (2010) Hyoungsu Kim et al. ORGANIC LETTERS
- Stereoselective Synthesis of Substituted Tetrahydropyrans via Domino Olefin Cross-Metathesis/Intramolecular Oxa-Conjugate Cyclization
- (2010) Haruhiko Fuwa et al. ORGANIC LETTERS
- Synthesis of the Tetrahydropyran Subunit (C8-C20 Fragment) of (-)-Dactylolide and (-)-Zampanolide
- (2010) Ch. Reddy et al. SYNLETT
- Stereoselective formal synthesis of aspergillide A
- (2010) Gowravaram Sabitha et al. TETRAHEDRON LETTERS
- Synthesis of the methylene bis-tetrahydropyran motif of (−)-exiguolide
- (2010) Ch. Raji Reddy et al. TETRAHEDRON LETTERS
- Stereoselective synthesis of the C1–C13 fragment of bistramide A
- (2010) Marie-Aude Hiebel et al. TETRAHEDRON LETTERS
- Organocatalysis in Natural Product Synthesis: A Simple One-Pot Approach to Optically Active β-Diols
- (2009) Nikolaj Røjkjær Andersen et al. ADVANCED SYNTHESIS & CATALYSIS
- Asymmetric Synthesis of Fluorinated Flavanone Derivatives by an Organocatalytic Tandem Intramolecular Oxa-Michael Addition/Electrophilic Fluorination Reaction by Using Bifunctional Cinchona Alkaloids
- (2009) Hai-Feng Wang et al. CHEMISTRY-A EUROPEAN JOURNAL
- Total Synthesis of (+)-Sorangicin A
- (2009) Amos B. Smith et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- An Efficient, Second-Generation Synthesis of the Signature Dioxabicyclo[3.2.1]octane Core of (+)-Sorangicin A and Elaboration of the (Z,Z,E)-Triene Acid System
- (2009) Amos B. Smith et al. ORGANIC LETTERS
- Tandem Ruthenium-Catalyzed Redox Isomerization−O-Conjugate Addition: An Atom-Economic Synthesis of Cyclic Ethers
- (2009) Barry M. Trost et al. ORGANIC LETTERS
- Organocatalytic Synthesis of an Alkyltetrahydropyran
- (2009) D. Díez et al. SYNLETT
- A carbohydrate approach for the synthesis of tetrahydropyran containing C16–C29 fragment of sorangicin A
- (2009) P. Srihari et al. TETRAHEDRON
- Synthesis of tetrahydropyrans and related heterocycles via prins cyclization; extension to aza-prins cyclization
- (2009) Clarisse Olier et al. TETRAHEDRON
- The oxa-Michael reaction: from recent developments to applications in natural product synthesis
- (2008) Carl F. Nising et al. CHEMICAL SOCIETY REVIEWS
- Formal Synthesis of (−)-Kendomycin Featuring a Prins-Cyclization To Construct the Macrocycle
- (2008) Kevin B. Bahnck et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Au(I)- and Pt(II)-Catalyzed Cycloetherification of ω-Hydroxy Propargylic Esters
- (2008) Jef K. De Brabander et al. ORGANIC LETTERS
- Synthesis of six-membered oxygenated heterocycles through carbon–oxygen bond-forming reactions
- (2008) Igor Larrosa et al. TETRAHEDRON
- Highly chemo- and diastereoselective synthesis of substituted tetrahydropyran-4-ones via organocatalytic oxa-Diels–Alder reactions of acyclic α,β-unsaturated ketones with aldehydes
- (2008) Liang-Qiu Lu et al. TETRAHEDRON LETTERS
- Enantioselective synthesis of the tetrahydro-6H-benzo[c]chromenes via Domino Michael–Aldol condensation: control of five stereocenters in a quadruple-cascade organocatalytic multi-component reaction
- (2008) Prakash Kotame et al. TETRAHEDRON LETTERS
- 2,6-Disubstituted Tetrahydropyrans by Tandem Cross-Metathesis/Iodocyclisation
- (2007) Marie-Aude Hiebel et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk 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