Regiochemistry of vinyl phosphate/.beta.-keto phosphonate rearrangements in functionalized cyclohexanones and decalones
摘要:
Diethyl vinyl phosphates derived from simple alkyl-substituted cyclohexanones and cyclohexenones are known to rearrange to beta-keto phosphonates upon treatment with excess LDA. To establish the effect of oxygen-containing functional groups on this transformation, vinyl phosphates containing remote carbonyl groups or acetals have been studied. The rearrangement fails in the presence of unprotected carbonyl groups but proceeds in the presence of acetals. To establish the regiochemistry of this rearrangement in fused-ring systems, representative decalins were studied. Through use of various ketones and enones, the 2- and 4-phosphono 3-keto compounds have been prepared in both cis-and trans-fused decalin series.
Regiochemistry of vinyl phosphate/.beta.-keto phosphonate rearrangements in functionalized cyclohexanones and decalones
摘要:
Diethyl vinyl phosphates derived from simple alkyl-substituted cyclohexanones and cyclohexenones are known to rearrange to beta-keto phosphonates upon treatment with excess LDA. To establish the effect of oxygen-containing functional groups on this transformation, vinyl phosphates containing remote carbonyl groups or acetals have been studied. The rearrangement fails in the presence of unprotected carbonyl groups but proceeds in the presence of acetals. To establish the regiochemistry of this rearrangement in fused-ring systems, representative decalins were studied. Through use of various ketones and enones, the 2- and 4-phosphono 3-keto compounds have been prepared in both cis-and trans-fused decalin series.
Regiochemistry of vinyl phosphate/.beta.-keto phosphonate rearrangements in functionalized cyclohexanones and decalones
作者:Yi Zhong An、David F. Wiemer
DOI:10.1021/jo00027a055
日期:1992.1
Diethyl vinyl phosphates derived from simple alkyl-substituted cyclohexanones and cyclohexenones are known to rearrange to beta-keto phosphonates upon treatment with excess LDA. To establish the effect of oxygen-containing functional groups on this transformation, vinyl phosphates containing remote carbonyl groups or acetals have been studied. The rearrangement fails in the presence of unprotected carbonyl groups but proceeds in the presence of acetals. To establish the regiochemistry of this rearrangement in fused-ring systems, representative decalins were studied. Through use of various ketones and enones, the 2- and 4-phosphono 3-keto compounds have been prepared in both cis-and trans-fused decalin series.