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DOI : 10.1021/ja00083a066

P. A. Wender, T. E. Glass, N. E. Krauss, M. Mühlebach, B. Peschke et al., The Pinene Path to Taxanes. 4. Approaches to Taxol and Taxol Analogs through Elaboration of Aromatic C-Ring Precursors, The Journal of Organic Chemistry, vol.61, issue.22, pp.7662-7663, 1996.
DOI : 10.1021/jo961289z

. Scheme-1, Olefin metathesis as dancers In 1971 Chauvin and his student Jean-Louis Hérisson showed how the metal-atom catalyst coordinates the rearrangement of carbon-carbon bonds (Scheme-1.28). 96 The catalytic cycle consists of a sequence of metathetical, p.92

T. Kanemitsu and P. H. Seeberger, Use of Olefin Cross-Metathesis to Release Azide-Containing Sugars from Solid Support, Organic Letters, vol.5, issue.24, pp.4541-4544, 2003.
DOI : 10.1021/ol035463z

C. Nmr, 6 MHz): ? (ppm) 159, 145.7 (C-Ar), pp.55-58

C. Diol, 21 mmol) was dissolved in MeOH (5 mL) at 20°C. Amberlyst H-15 (40 mg) was then added, and the mixture was stirred overnight at 20°C. The resin was then filtered off and the solvents were removed in vacuo. Purification of the crude product by flash chromatography, 82% yield) as a colorless oil

1. Hzdt and J. =. , 21 (s, 1H, pp.6-11

1. Ddd, 1. , 2. , and J. =. , 72 (m, 1H, H-10), 5.25-5.20 (m, 2H, H-2'), 5.09-5.01 (m, 3H, H-1, NMR (CDCl 3 , 400 MHz): ? (ppm) 6.03, pp.9582-57466, 1927.