Literature DB >> 12770589

The absolute stereochemistry of a diterpene from Ballota aucheri.

Christopher A Gray1, Douglas E A Rivett, Michael T Davies-Coleman.   

Abstract

The semi-synthetic transformation of hispanolone, isolated from Ballota africana, into 6beta-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one has established an ent-labdane absolute stereochemistry for a diterpene metabolite originally isolated from B. aucheri.

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Year:  2003        PMID： 12770589     DOI： 10.1016/s0031-9422(03)00156-0

Source DB:  PubMed          Journal:  Phytochemistry        ISSN： 0031-9422            Impact factor:   4.072


  4 in total

1.  New diterpenoids with estrogen sulfotransferase inhibitory activity from Leonurus sibiricus L.

Authors:  Yuji Narukawa; Akiko Niimura; Hitomi Noguchi; Hiroomi Tamura; Fumiyuki Kiuchi
Journal:  J Nat Med       Date:  2013-06-05       Impact factor: 2.343

2.  A database-driven approach identifies additional diterpene synthase activities in the mint family (Lamiaceae).

Authors:  Sean R Johnson; Wajid Waheed Bhat; Jacob Bibik; Aiko Turmo; Britta Hamberger; Björn Hamberger
Journal:  J Biol Chem       Date:  2018-11-29       Impact factor: 5.157

Review 3.  The Botanical, Chemical and Ethnobotanical Diversity of Southern African Lamiaceae.

Authors:  Ryan D Rattray; Ben-Erik Van Wyk
Journal:  Molecules       Date:  2021-06-18       Impact factor: 4.411

4.  Expanding the Landscape of Diterpene Structural Diversity through Stereochemically Controlled Combinatorial Biosynthesis.

Authors:  Johan Andersen-Ranberg; Kenneth Thermann Kongstad; Morten Thrane Nielsen; Niels Bjerg Jensen; Irini Pateraki; Søren Spanner Bach; Britta Hamberger; Philipp Zerbe; Dan Staerk; Jörg Bohlmann; Birger Lindberg Møller; Björn Hamberger
Journal:  Angew Chem Int Ed Engl       Date:  2016-01-08       Impact factor: 15.336
  4 in total

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