Synthesis of (+/-)-Conduramines from Pyrrole

DOI: 10.1016/0040-4039(94)88307-6

Source and publish data:

Tetrahedron Letters p. 1639 - 1642 (1994)

Update date:2022-08-05

Topics:

Authors:

Leung-Toung, Regis

Liu, Yanzhou

Muchowski, Joseph M.

Wu, Yu-Lin

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Article abstract of DOI:10.1016/0040-4039(94)88307-6

The Diels-Alder product 1b, of tosylacetylene and N-tert-Boc-pyrrole, was converted into (+/-)-conduramine C-1 (22) and the tetraacetates of (+/-)-conduramine A-1 (9b) and F-1 (15b).

Full text of DOI:10.1016/0040-4039(94)88307-6

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Product name:(+/-)-1-p-toluenesulfonyl-5-tert-butoxycarbonylamino-1,3-cyclohexadiene

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