Rearrangement of thiazolidine derivatives – a synthesis of a chiral fused oxathiane–γ-lactam bicyclic system
文献情報
Karolina Kamińska, Dominika Iwan, Jakub Trojnar, Marek Daszkiewicz, Joanna E. Rode, Jacek Wojaczyński, Elżbieta Wojaczyńska
Reaction of L-cysteine with carbonyl compounds leads to thiazolidine derivatives which undergo a stereoselective conversion to two types of chiral bicyclic products bearing two or three stereogenic centers, including the first fused oxathiane–γ-lactam system.
おすすめジャーナル

Polycyclic Aromatic Compounds

Acta Metallurgica Sinica-English Letters

Bioorganic & Medicinal Chemistry

Biocatalysis and Biotransformation

Colloid Journal

Journal of Asian Natural Products Research

Journal of Chemical Sciences

Medicinal Chemistry Research

Critical Reviews in Solid State and Materials Sciences

Electroanalysis
関連文献
Ionic diamine rhodium(i) complexes—highly active catalysts for the hydroformylation of olefins
Jai Jun Kim, Howard Alper
DOI: 10.1039/B502435H
Figure-eight aromatic core-modified octaphyrins with six meso links: syntheses and structural characterization
Harapriya Rath, Jeyaraman Sankar, Viswanathan PrabhuRaja, Tavarekere K. Chandrashekar, Bhawani S. Joshi, Raja Roy
DOI: 10.1039/B502327K
Quenching of CdSe quantum dot emission, a new approach for biosensing
L. Dyadyusha, H. Yin, S. Jaiswal, T. Brown, J. J. Baumberg, F. P. Booy
DOI: 10.1039/B500664C
Synthesis of huge macrocycles using two calix[4]arenes as templates
Yudong Cao, Leyong Wang, Michael Bolte, Myroslav O. Vysotsky, Volker Böhmer
DOI: 10.1039/B505223H
Reversible hydrogen gas uptake in nanoporous Prussian Blue analogues
Karena W. Chapman, Peter D. Southon, Colin L. Weeks, Cameron J. Kepert
DOI: 10.1039/B502850G
Enantioselective segregation in achiral nematic liquid crystals
DOI: 10.1039/B503846D
Discrete dispersion of single-walled carbon nanotubes
Qingwen Li, Ian A. Kinloch, Alan H. Windle
DOI: 10.1039/B419039D
Enantioselective total synthesis of a novel polyketide natural product (+)-integrasone, an HIV-1 integrase inhibitor
Goverdhan Mehta, Subhrangsu Roy
DOI: 10.1039/B502024G
Theoretical studies on di- and tetra-nuclear Ni pivalate complexes
Gopalan Rajaraman, Kirsten E. Christensen, Finn K. Larsen, Grigore A. Timco, R. E. P. Winpenny
DOI: 10.1039/B502115D
こちらもおすすめ
6-苄基-6,7-二氢-5H-吡咯并3,4-b吡啶とは何ですか?
6-苄基-6,7-二氢-5H-吡咯并3,4-b吡啶は、CAS番号109966-30-5の化合物です。これは、6-ベンジル基を持つ6,7-二氢-5H-吡咯並みの化...
半硫酸奎宁单水水合物はどのように保存すればよいですか?
半硫酸奎宁单水水合物は、乾燥した涼しい場所に保管し、直射日光や湿気を避ける必要があります。保存温度は常温(15〜25℃)が適切で、湿度は40%以下を維持すること...
D-核糖-5-リン酸二ナトリウムとは何ですか?
D-核糖-5-リン酸二ナトリウムは、CAS番号18265-46-8を有する化合物で、D-核糖の5位付加部位にリン酸基が結合した化合物です。この化合物は、水溶性で...
3-乙酰基-4-羟基喹啉-2(1H)-酮はどのように合成されますか?
3-乙酰基-4-羟基喹啉-2(1H)-酮は、ハイドロキノンと酢酸アセトイルアミドのアミド化反応により合成されます。この反応は塩基触媒を用いて行われ、選択性は良好...
5-溴-4-甲基-1H-吲唑とは何ですか?
5-溴-4-甲基-1H-吲唑は、CAS番号1082041-34-6の化学物質で、化学式はC10H9BrNです。この化合物は淡黄色の結晶性粉末で、吸湿性があります...
3-(4メトキシフェニル)オキテナン-3カーボイル酸の代替品はありますか?
3-(4メトキシフェニル)オキテナン-3カーボイル酸の代替品は、その用途により異なりますが、例えば4-(メトキシフェニル)オキテナン-3カーボイル酸や、他のオキ...
3-イリドオキシピロロ[2,3-b]ピリジン-5-カルボキシlic酸は安全ですか?
3-イリドオキシピロロ[2,3-b]ピリジン-5-カルボキシlic酸は危険な化合物ではありませんが、適切な手袋や保護眼鏡の使用を推奨します。誤って摂取または接触...
3-氟-4- iodobenolを取り扱う際の実験室安全事項は何ですか?
3-氟-4- iodobenolは可燃性を有し、強力な反応性を持つため、取り扱いには注意が必要です。PPE(個人保護具)の着用、ドラフトチャンバーの使用、漏洩時...
掲載誌
Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.




