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28
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85029996054
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We thank Professor Kosta Steliou of Boston University for providing a copy of the extensively rewritten Still Model program and for providing a VMS version of MMX
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We thank Professor Kosta Steliou of Boston University for providing a copy of the extensively rewritten Still Model program and for providing a VMS version of MMX.
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85029993910
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note
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The results obtained with 26 show that there must be reversible formation of the 1,3-dipole, since in the absence of the dipolarophile, the non 1,3-dipole products are formed in 77% yield, whereas in the presence of N-phenyl maleimide, a 60-100% yield of the 1,3-dipolar cycloadduct is formed.
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