1. Synthesis of Ether Analogues of (±)-Acetomycin
Huw M. L. Davies and Baihua Hu
Heterocycles
Special issue | Vol 35, No. 1, 1993, pp.385-393
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http://dx.doi.org/10.3987/COM-92-S32
2. Enantioselective syntheses of polyhydroxylated nortropane derivatives: Total synthesis of (+) and (−)-calystegine B2
François-Didier Boyer, Jean-Yves Lallemand
Tetrahedron
Volume 50, Issue 35, 1994, Pages 10443–10458
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http://dx.doi.org/10.1016/S0040-4020(01)89584-3
3. Tigliane Type Diterpene-esters with Epstein-Barr Virus-inducing Activity from Sapium sebiferum
Hajime OHIGASHI, Takanao OHTSUKA, Mitsuru HIROTA, Koichi KOSHIMIZU, Harukuni TOKUDA, Yohei ITO
Agricultural and Biological Chemistry
Vol. 47 (1983) No. 7 P 1617-1622
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http://dx.doi.org/10.1271/bbb1961.47.1617
4. Chemistry with Stress and Strain: New Cyclopropyl Building Blocks For Organic Synthesis
Armin De Meijere
Bulletin des Sociétés Chimiques Belges
Volume 93, Issue 3, pages 241–260, 1984
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http://dx.doi.org/10.1002/bscb.19840930313
5. The crystal structure of 2β,4β-cyclo-5α-androstane-3α, 17β-diol diacetate
James C. Orr, Michael J. Newlands, Eric J. Gabe, Jean-Pierre Charland
Steroids
Volume 52, Issues 1–2, July–August 1988, Pages 37–43
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http://dx.doi.org/10.1016/0039-128X(88)90215-2
Kalapati Seshadri, Perali Ramu Sridhar
Synthesis 2014; 46(07): 923-932
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http://dx.doi.org/10.1055/s-0033-1340617
Russell J. Hewitt and Joanne E. Harvey
Org. Biomol. Chem., 2011,9, 998-1000
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http://dx.doi.org/10.1039/C0OB00851F
Setsuya Sasho1), Takashi Seishi, Mariko Kawamura, Misato Tomuro, Ryo Hirose, Shinichiro Toki, Junich Shimada
Chemical and Pharmaceutical Bulletin
Vol. 57 (2009) No. 3 P 288-293
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http://dx.doi.org/10.1248/cpb.57.288