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1. Silylmethyl-substituted cyclopropyl and other strained ring systems: cycloaddition with dipolarophiles
Chem. Commun., 2008, 6471-6488
- DOI:
http://dx.doi.org/10.1039/B812285G
2. 1,2-Asymmetric rearrangements in chiral sulfinylcyclopropane systems: asymmetric synthesis of .alpha.,.alpha.-disubstituted cyclobutanones
J. Am. Chem. Soc., 1987, 109 (4), pp 1249–1250
- DOI:
http://dx.doi.org/10.1021/ja00238a047
3. Dynamic behaviour of carbocations on zeolites: mobility and rearrangement of the C4H7+ system
Chem. Commun., 2013,49, 4480-4482
- DOI:
http://dx.doi.org/10.1039/C3CC40627J
4. Small-ring Compounds. XXIII. The Nature of the Intermediates in Carbonium Ion-type Interconversion Reactions of Cyclopropylcarbinyl, Cyclobutyl and Allylcarbinyl Derivatives1a
J. Am. Chem. Soc., 1959, 81 (16), pp 4390–4398
- DOI:
http://dx.doi.org/10.1021/ja01525a073
5. Low-temperature carbon-13 nuclear magnetic resonance spectroscopic investigation of C4H7+. Evidence for an equilibrium involving the nonclassical bicyclobutonium ion and the bisected cyclopropylcarbinyl cation
J. Am. Chem. Soc., 1978, 100 (25), pp 8016–8018
- DOI:
http://dx.doi.org/10.1021/ja00493a045
6. Synthesis of γ-methylene oxacycles and α- and β-alkylidene lactones via silicon-assisted ring opening of cyclopropyl carbinols
Chem. Commun., 2002, 514-515
- DOI:
http://dx.doi.org/10.1039/B111332C
7. Letters in Organic Chemistry
Evaluation of Sulfonamides in the Protection of Phenylisoserine for the Semisynthesis of Taxol®
Peter G.M. Wuts, Rui L. Gu and Jill M. Northuis
Pages 372-375 (4)
- DOI:
http://dx.doi.org/10.2174/1570178043400587
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