Rearrangement of Isoxazoline-5-spiro Derivatives. 5. Diastereofacial Selectivity in the Cycloaddition of Substituted Five-Membered Cyclic Nitrones and Methylenecyclopropanes. Srereoselective Synthesis of 3,5-Substituted Indolizidinones

DOI: 10.1021/jo00293a018

Source and publish data:

Journal of Organic Chemistry p. 1762 - 1767 (1990)

Update date:2022-09-26

Topics:

Authors:

Cordero, Franca M.

Brandi, Alberto

Querci, Cecilia

Goti, Andrea

Sarlo, Francesco De

Guarna, Antonio

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Article abstract of DOI:10.1021/jo00293a018

Substituted five-membered cyclic nitrones 1-3 cycloadd to substituted methylenecyclopropanes 4 and 5 with high diasrereofacial selectivity, through anti-anti transition states, to produce regioisomeric hexahydrospiro View More

Full text of DOI:10.1021/jo00293a018

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