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. Author manuscript; available in PMC: 2010 Apr 5.
Published in final edited form as: J Am Chem Soc. 2009 Aug 5;131(30):10652–10661. doi: 10.1021/ja904098h

Table 2.

Selective Synthesis of endo-Carbocyclic Dienes by Mo-Catalyzed Enyne RCM (Acetonide Tether)a-d

entry substrate endo product exo product endo:exob yield (%)c
1 graphic file with name nihms-173123-t0026.jpg graphic file with name nihms-173123-t0027.jpg graphic file with name nihms-173123-t0028.jpg >98:<2 81
2 graphic file with name nihms-173123-t0029.jpg graphic file with name nihms-173123-t0030.jpg graphic file with name nihms-173123-t0031.jpg 75:25 75d
3 graphic file with name nihms-173123-t0032.jpg graphic file with name nihms-173123-t0033.jpg graphic file with name nihms-173123-t0034.jpg 66:33 72d
4 graphic file with name nihms-173123-t0035.jpg graphic file with name nihms-173123-t0036.jpg graphic file with name nihms-173123-t0037.jpg >98:<2 81
a

Reactions were performed under N2 atmosphere with 5 mol % 5 for 30 min in C6H6 at 22 °C.

b

Ratios were determined by analysis of 400 MHz 1H NMR spectra of unpurified mixtures prior to purification.

c

Yield of isolated products after purification.

d

Combined yields of the product mixture.