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- Syntheses of 2-ethyl-8-methyl-1,7-dioxaspiro[5.5]undecanols. Mark F. Jacobs, Bill D. Suthers, Achim Hübener, William Kitching
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 901
- Isolation and synthesis of 1,7-dioxaspiro[5.5]undecane and 1,7-dioxaspiro[5.5]undecan-3-and -4-ols from the olive fly (Dacus oleae). Raymond Baker, Richard H. Herbert
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 1123
- Synthesis of talaromycins A, B, C, and E. Raymond Baker, Alastair L. Boyes, Christopher J. Swain
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1415
- Synthesis of spiroacetals using organoselenium-mediated cyclisation reactions. X-Ray molecular structure of (2S,8R)-8-methyl-2-phenyl-1,7-dioxaspiro[5.5]undecan-4(R)-ol. Annette M. Doherty, Steven V. Ley, Barry Lygo, David J. Williams
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 1371
- The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the AB-spiroacetal segment. Ian Paterson, Mark J. Coster, David Y.-K. Chen, Renata M. Oballa, Debra J. Wallace, Roger D. Norcross
, Org. Biomol. Chem.
, 2005
, 3
, 2399
- Biosynthesis of insect spiroacetals. Yvonne K. Booth, William Kitching, James J. De Voss
, Nat. Prod. Rep.
, 2009
, 26
, 490
- Synthetic approaches to the C11–C27 fragments of bryostatins. Anthony P. Green, Simon Hardy, Eric J. Thomas
, Org. Biomol. Chem.
, 2017
, 15
, 9475
- The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the CD-spiroacetal segment. Ian Paterson, Mark J. Coster, David Y.-K. Chen, Karl R. Gibson, Debra J. Wallace
, Org. Biomol. Chem.
, 2005
, 3
, 2410
- [1,4]-sigmatropic rearrangement of chiral nitrones and their utilization in the synthesis of new iminosugars. Maciej Malinowski, Tomasz Rowicki, Patrycja Guzik, Maciej Gryszel, Sebastian Łapczyński, Monika Wielechowska, Karolina Czerwińska, Izabela Madura, Wojciech Sas
, Org. Biomol. Chem.
, 2016
, 14
, 470
- Synthesis based on cyclohexadienes. Part 25.1 Total synthesis of (±)-allo-cedrol (khusiol). P. Sathya Shanker, G. S. R. Subba Rao
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 539