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- Enzymatic synthesis of cyclic triterpenes. Ikuro Abe
, Nat. Prod. Rep.
, 2007
, 24
, 1311
- Lichens and fungi. Part XI. Isolation and structural elucidation of a new group of triterpenes from Sticta coronata, S. colensoi, and S. flavicans. Wah J. Chin, R. Edward Corbett, Ching K. Heng, Alistair L. Wilkins
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 1437
- Lichens and fungi. Part II. Isolation and structural elucidation of 7β-acetoxy-22-hydroxyhopane from Sticta billardierii Del.. R. E. Corbett, H. Young
, J. Chem. Soc. C
, 1966
, 1556
- Mutated variants of squalene-hopene cyclase: enzymatic syntheses of triterpenes bearing oxygen-bridged monocycles and a new 6,6,6,6,6-fusded pentacyclic scaffold, named neogammacerane, from 2,3-oxidosqualene. Yoriyuki Fukuda, Takashi Watanabe, Tsutomu Hoshino
, Org. Biomol. Chem.
, 2018
, 16
, 8365
- Bacterial triterpenes. M. De Rosa, A. Gambacorta, L. Minale, J. D. Bu'Lock
, J. Chem. Soc. D
, 1971
, 619
- Lichens and fungi. Part IX. 17αH-hopane and 17αH-moretane and their derivatives. R. E. Corbett, C. K. Heng
, J. Chem. Soc. C
, 1971
, 1885
- Lichens and Fungi. Part IV. Rearrangements at C-21 in the hopane series. R. E. Corbett, R. A. J. Smith
, J. Chem. Soc. C
, 1967
, 1622
- Squalene–hopene cyclase: insight into the role of the methyl group on the squalene backbone upon the polycyclization cascade. Enzymatic cyclization products of squalene analogs lacking a 26-methyl group and possessing a methyl group at C(7) or C(11). Shin-ichi Nakano, Shumi Ohashi, Tsutomu Hoshino
, Org. Biomol. Chem.
, 2004
, 2
, 2012
- The cyclization mechanism of squalene in hopene biosynthesis: the terminal methyl groups are critical to the correct folding of this substrate both for the formation of the five-membered E-ring and for the initiation of the polycyclization reaction†. Tsutomu Hoshino
, Chem. Commun.
, 1999
, 731
- Biosynthesis of terpenes and steroids. Part III. Squalene cyclisation in the biosynthesis of triterpenoids; the biosynthesis of fern-9-ene in Polypodium vulgare Linn. D. H. R. Barton, G. Mellows, D. A. Widdowson
, J. Chem. Soc. C
, 1971
, 110