STUDIES ON THE SYNTHESIS OF NARGENICIN A1. AN EXAMPLE OF AN INTRAMOLECULAR DIELS-ALDER REACTION THAT PROCEEDS WITH A BOAT-LIKE CONFORMATION OF THE CONNECTING CHAIN

DOI: 10.1016/S0040-4039(00)95877-5

Source and publish data:

Tetrahedron Letters p. 931 - 934 (1987)

Update date:2022-08-03

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Authors:

Roush, William R.

Coe, Jotham W.

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Article abstract of DOI:10.1016/S0040-4039(00)95877-5

The intramolecular Diels-Alder reaction of triene 2 proceeds with excellent stereoselectivity via boat transition state B and provides cycloadduct 4 in 78percent yield.

Full text of DOI:10.1016/S0040-4039(00)95877-5

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