ASYMMETRIC DIELS-ALDER REACTIONS OF A NITROSO COMPOUND DERIVED FROM D-BORNANE-10,2-SULTAM

ASYMMETRIC DIELS-ALDER REACTIONS OF A NITROSO COMPOUND DERIVED FROM D-BORNANE-10,2-SULTAM

Acylnitroso dienophile 3 derived from D-bornane-10,2-sultam undergoes cycloaddition with high yields and complete facial selectivity to cyclopentadiene and cyclohexadiene. When the nitroso group is attached to the sultam nitrogen, it is no longer reactive in Diels-Alder reactions. © 1991.

書誌詳細
主要な著者:	Gouverneur, V, Dive, G, Ghosez, L
フォーマット:	Journal article
出版事項:	1991

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