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- Ajmaline. Part I. F. A. L. Anet, D. Chakravarti, Robert Robinson, E. Schlittler
, J. Chem. Soc.
, 1954
, 1242
- 739. On the origin of the C-1 fragment in indole alkaloids. D. H. R. Barton, G. W. Kirby, R. H. Prager, E. M. Wilson
, J. Chem. Soc.
, 1965
, 3990
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The impact of structural biology on alkaloid biosynthesis research. Santosh Panjikar, Joachim Stoeckigt, Sarah O'Connor, Heribert Warzecha
, Nat. Prod. Rep.
, 2012
, 29
, 1176
- Structural biology in plant natural product biosynthesis—architecture of enzymes from monoterpenoid indole and tropane alkaloid biosynthesis. Joachim Stöckigt, Santosh Panjikar
, Nat. Prod. Rep.
, 2007
, 24
, 1382
- The total synthesis of (−)-suaveoline. Patrick D. Bailey, Keith M. Morgan
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 3578
- Cleavage of tertiary bases with phenyl chloroformate: the reconversion of 21-deoxyajmaline into ajmaline. J. D. Hobson, J. G. McCluskey
, J. Chem. Soc. C
, 1967
, 2015
- Biosynthesis of the C9–10 unit of ajmaline and reserpine. A. K. Garg, J. R. Gear
, J. Chem. Soc. D
, 1969
, 1447
- Trends for diverse production strategies of plant medicinal alkaloids. Liuqing Yang, Joachim Stöckigt
, Nat. Prod. Rep.
, 2010
, 27
, 1469
- Stereoselective transformation of ajmaline into three minor Gelsemium alkaloids, koumidine, (19Z)-anhydrovobasinediol [(19Z)-taberpsychine] and N-demethoxyrankinidine and their absolute configuration. Mariko Kitajima, Hiromitsu Takayama, Shin-ichiro Sakai
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 1773
- New asymmetric routes to ajmaline and suaveoline indole alkaloids. Patrick D. Bailey, Keith M. Morgan, David I. Smith, John M. Vernon
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 3566