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- Group-theoretical framework for characterizing the ring flipping of spiro[5.5]undecane derivatives. Pseudo-point groups and subsymmetry-itemized enumeration. Shinsaku Fujita
, J. Chem. Soc., Faraday Trans.
, 1998
, 94
, 3197
- A new domino autocatalytic reaction leading to polyfunctionalized spiro[5.5]undecanes and dispiro[4.2.5.2]pentadecanes. Bo Jiang, Wen-Juan Hao, Jin-Peng Zhang, Shu-Jiang Tu, Feng Shi
, Org. Biomol. Chem.
, 2009
, 7
, 2195
- Biosynthesis of insect spiroacetals. Yvonne K. Booth, William Kitching, James J. De Voss
, Nat. Prod. Rep.
, 2009
, 26
, 490
- Synthesis of highly substituted 2-spiropiperidines. Samuel D. Griggs, Nathan Thompson, Daniel T. Tape, Marie Fabre, Paul A. Clarke
, Org. Biomol. Chem.
, 2018
, 16
, 6663
- Conformation analysis of spiranes by the force-field method. Part 1. Chirality and diastereoisomerism of spiro-compounds: spiro[5.5]undecane and derivatives. Helena Dodziuk
, J. Chem. Soc., Perkin Trans. 2
, 1986
, 249
- Spiro[5.5]undecane sesquiterpene analogues. Bridging vinyl ether and vinyl acetal formation via intramolecular attack by an enol during bromination. Lorenzo P. L. Piacenza
, J. Chem. Soc., Chem. Commun.
, 1978
, 425
- Alkynylation/dearomatizative cyclization to construct spiro[5.5]undecanes. Jidong Shao, Liqi Li, Jie Zhang, Jingping Hu, Jijun Xue, Ying Li
, RSC Adv.
, 2016
, 6
, 31363
- Diverted organic synthesis (DOS): accessing a new, natural product inspired, neurotrophically active scaffold through an intramolecular Pauson–Khand reaction. Goverdhan Mehta, Ramesh Samineni, Pabbaraja Srihari, R. Gajendra Reddy, Sumana Chakravarty
, Org. Biomol. Chem.
, 2012
, 10
, 6830
- Design, synthesis and biological evaluation of optically pure functionalized spiro[5,5]undecane-1,5,9-triones as HIV-1 inhibitors. Dhevalapally B. Ramachary, Y. Vijayendar Reddy, Atoshi Banerjee, Sharmistha Banerjee
, Org. Biomol. Chem.
, 2011
, 9
, 7282
- Synthesis and elaboration of functionalised carbohydrate-derived spiroketals. Peter A. V. van Hooft, Farid El Oualid, Herman S. Overkleeft, Gijsbert A. van der Marel, Jacques H. van Boom, Michiel A. Leeuwenburgh
, Org. Biomol. Chem.
, 2004
, 2
, 1395