Enantioselective total synthesis of (−)-heliannuol A

Literature Information

Publication Date 2003-01-09
DOI 10.1039/B211227B
Impact Factor 6.222
Authors

Hidetoshi Kishuku, Mitsuru Shindo, Kozo Shishido


View Original

Abstract

An efficient and enantiocontrolled total synthesis of (−)-heliannuol A has been accomplished by employing ring closing metathesis and sequential diastereoselective epoxidation and regioselective reductive cleavage of the epoxide ring.

Related Literature

Tailored monolith supports for improved ultra-low temperature water-gas shift reaction

Raquel Portela, Patrick Wolf, Jakob M. Marinkovic, Ana Serrano-Lotina, Anders Riisager, Marco Haumann

2021-08-03 Paper

DOI: 10.1039/D1RE00226K

Concentric annular liquid–liquid phase separation for flow chemistry and continuous processing

Bin Feng, Heather O'Connor, Denis Dowling, Geoff Gibson, Kevin P. Girard

2021-06-24 Paper

DOI: 10.1039/D1RE00119A

Exponential growth of functional poly(glutamic acid)dendrimers with variable stereochemistry

Sebastian Hartwig, Mary M. Nguyen, Stefan Hecht

2009-11-25 Communication

DOI: 10.1039/B9PY00217K

Kinetic and mechanistic insights into Ni-AlKIT-6 catalyzed ethylene oligomerization

Remi Beucher, Vasile Hulea, Claudia Cammarano

2021-10-11 Paper

DOI: 10.1039/D1RE00258A

Hyperbranched 5,6-glucan as reducing sugar ball

Masaki Tamaki, Tsukasa Taguchi, Soichi Nakabayashi, Kota Mori, Yoshikazu Kitajyo, Ryosuke Sakai, Toyoji Kakuchi, Toshifumi Satoh

2009-12-21 Paper

DOI: 10.1039/B9PY00223E

Multi-scale reactive extrusion modelling approaches to design polymer synthesis, modification and mechanical recycling

Kyann De Smit, Yoshi W. Marien, Paul H. M. Van Steenberge, Mariya Edeleva

2022-01-11 Review Article

DOI: 10.1039/D1RE00556A

Selective separation of amines from continuous processes using automated pH controlled extraction

Luke A. Power, Adam D. Clayton, William R. Reynolds, David R. J. Hose, Caroline Ainsworth, Thomas W. Chamberlain, Bao N. Nguyen, Richard A. Bourne, Nikil Kapur, A. John Blacker

2021-08-25 Communication

DOI: 10.1039/D1RE00205H

Catalyst-free valorization of poly-3-hydroxybutyrate to crotonic acid

Shimin Kang, Jinxia Fu, Jianhao Liang, Suxia Chen, Lijun Lu, Rongrong Miao

2021-08-02 Communication

DOI: 10.1039/D1RE00273B

You might also like

Compound Q&A

What precautions should be taken when handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2)?

When handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2), it is importan...

16712-20-2Lithium chloride hyd...
Compound Q&A

Is 4-(4H-1,2,4-Triazol-4-yl)piperidine (CAS: 690261-92-8) safe?

4-(4H-1,2,4-Triazol-4-yl)piperidine is generally considered safe for use in phar...

690261-92-84-(4H-1,2,4-Triazol-...
Compound Q&A

How should waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) be handled?

Waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) should be collecte...

16733-85-01,3-Thiazole-2-carbo...
Compound Q&A

What regulatory guidelines apply to 5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3)?

5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3) is subject to regulat...

934175-58-35-(Difluoromethyl)-2...
Compound Q&A

How is Methyl 3-acetamido-2-thiophenecarboxylate (CAS: 22288-79-5) typically synthesized?

Methyl 3-acetamido-2-thiophenecarboxylate can be synthesized by the reaction of ...

22288-79-5Methyl 3-acetamido-2...
Compound Q&A

What is 4-Isoquinolinecarbonitrile (CAS: 34846-65-6)?

4-Isoquinolinecarbonitrile is a chemical compound with the CAS number 34846-65-6...

34846-65-64-Isoquinolinecarbon...
Compound Q&A

How should Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) be stored?

Store Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) in a cool, dry p...

877309-59-6Methyl 1H-1,2,3-tria...
Compound Q&A

What regulatory guidelines apply to 6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8)?

6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8) is subject to the...

1160791-13-86-Bromo[1,3]thiazolo...
Compound Q&A

Is (2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) safe?

(2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) ...

23651-95-8(2S,3S)-2-Ammonio-3-...
Compound Q&A

What are the physical and chemical properties of 7-bromo-3-methyl-3,4-dihydroquinazolin-4-one (CAS: 1293987-84-4)?

7-Bromo-3-methyl-3,4-dihydroquinazolin-4-one is a solid with a crystalline form....

1293987-84-47-bromo-3-methyl-3,4...

Source Journal

Chemical Communications

Chemical Communications
CiteScore: 8.6
Self-citation Rate: 4.7%
Articles per Year: 2458

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.