Substituted phenoxy acetyl chloride reacted with trimethyl phosphite to form an unexpected substituted phenoxy acetic acid ester, confirmed by ~1HNMR, IR and MS. The mechanism suggested is different from that of Arbuz...Substituted phenoxy acetyl chloride reacted with trimethyl phosphite to form an unexpected substituted phenoxy acetic acid ester, confirmed by ~1HNMR, IR and MS. The mechanism suggested is different from that of Arbuzov reaction.展开更多
Title compounds 2′,2′-dimethylcholesta-2,4-dien[3,2-b]-pyran-4′-one （3）, 2′,2′-dimethyl-3β-substituted cholesta-4,6-dien[7,6- b]-pyran-4′-one （6a,b） and （6c） were prepared by the cyclization of 2-acetylch...Title compounds 2′,2′-dimethylcholesta-2,4-dien[3,2-b]-pyran-4′-one （3）, 2′,2′-dimethyl-3β-substituted cholesta-4,6-dien[7,6- b]-pyran-4′-one （6a,b） and （6c） were prepared by the cyclization of 2-acetylcholesta-2,4-dien-3-ol （2）, 6-acetyl-3β-substituted- cholesta-4,6-dien-7-ol （Sa,b） and （5c） respectively, with pyrrolidine, dry benzene and dry acetone using Dean Stark separator through conventional heating. Furthermore, compounds were also found to be active against Mycobacterium tuberculosis.展开更多
A convenient method has been developed for the synthesis of diphenyl α-（dipropoxyphosphoramido）alkyl- phosphonates under mild conditions, namely the reaction of dipropyl phosphoramidate （1） with a para（un）subst...A convenient method has been developed for the synthesis of diphenyl α-（dipropoxyphosphoramido）alkyl- phosphonates under mild conditions, namely the reaction of dipropyl phosphoramidate （1） with a para（un）substituted benzaldehyde or cyclicketone （2） and triphenyl phosphite （3） by a one-pot procedure with the aid of acetyl chloride.展开更多
文摘Substituted phenoxy acetyl chloride reacted with trimethyl phosphite to form an unexpected substituted phenoxy acetic acid ester, confirmed by ~1HNMR, IR and MS. The mechanism suggested is different from that of Arbuzov reaction.
文摘Title compounds 2′,2′-dimethylcholesta-2,4-dien[3,2-b]-pyran-4′-one （3）, 2′,2′-dimethyl-3β-substituted cholesta-4,6-dien[7,6- b]-pyran-4′-one （6a,b） and （6c） were prepared by the cyclization of 2-acetylcholesta-2,4-dien-3-ol （2）, 6-acetyl-3β-substituted- cholesta-4,6-dien-7-ol （Sa,b） and （5c） respectively, with pyrrolidine, dry benzene and dry acetone using Dean Stark separator through conventional heating. Furthermore, compounds were also found to be active against Mycobacterium tuberculosis.
文摘A convenient method has been developed for the synthesis of diphenyl α-（dipropoxyphosphoramido）alkyl- phosphonates under mild conditions, namely the reaction of dipropyl phosphoramidate （1） with a para（un）substituted benzaldehyde or cyclicketone （2） and triphenyl phosphite （3） by a one-pot procedure with the aid of acetyl chloride.
