Literature DB >> 14748605

Enantiocontrolled synthesis of jasmonates via tandem retro-Diels-Alder-ene reaction activated by a silyl substituent.

Katsufumi Suzuki1, Kohei Inomata, Yasuyuki Endo.   

Abstract

[reaction: see text] An enantiocontrolled synthesis of (-)-methyl 6-epi-cucurbate and (+)-methyl jasmonate was established from a chiral tricyclic lactone via a new type of tandem retro-Diels-Alder-ene reaction activated by a trimethysilyl substituent as the key step.

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Year:  2004        PMID: 14748605     DOI: 10.1021/ol036253p

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Continuous-flow retro-Diels-Alder reaction: an efficient method for the preparation of pyrimidinone derivatives.

Authors:  Imane Nekkaa; Márta Palkó; István M Mándity; Ferenc Fülöp
Journal:  Beilstein J Org Chem       Date:  2018-02-01       Impact factor: 2.883

2.  Jasmonic acid biosynthesis by fungi: derivatives, first evidence on biochemical pathways and culture conditions for production.

Authors:  Felipe Eng; Jorge Erick Marin; Krzysztof Zienkiewicz; Mariano Gutiérrez-Rojas; Ernesto Favela-Torres; Ivo Feussner
Journal:  PeerJ       Date:  2021-02-05       Impact factor: 2.984

3.  Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4]triazolo[4,3-a]pyrimidin-7(1H)-ones.

Authors:  Awad I Said; Márta Palkó; Matti Haukka; Ferenc Fülöp
Journal:  RSC Adv       Date:  2020-09-14       Impact factor: 4.036

  3 in total

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