The Journal of organic chemistry

Total synthesis of Amaryllidaceae pyrrolophenanthridinium alkaloids via the Ziegler-Ullmann reaction: Tortuosine, criasbetaine, and ungeremine

LM Stark, XF Lin, LA Flippin

Index: Stark, Lucy M.; Lin, Xiao-Fa; Flippin, Lee A. Journal of Organic Chemistry, 2000 , vol. 65, # 10 p. 3227 - 3230

Full Text: HTML

Citation Number: 37

Abstract

In connection with a program in our laboratory directed toward the total synthesis of pyrrolophenanthridinium alkaloids for antitumor screening, 2 we required a short and general approach to the Narcissus tortuosus constituent tortuosine, 1, 3 its structural relative criasbetaine, 2, 4 from Crinum asiaticum, and ungeremine, 3. 5 Structure-activity relationship (SAR) data for antitumor efficacy within the small class of known Amaryllidaceae ...

Related Articles:

A Novel Class of Inhibitors for Human and Rat Steroid 5. ALPHA.-Reductases: Synthesis and Biological Evaluation of Indoline and Aniline Derivatives. III.

[Igarashi; Inami; Hara; Koutoku; Oritani; Mase Chemical and Pharmaceutical Bulletin, 2000 , vol. 48, # 11 p. 1689 - 1697]

A Novel Class of Inhibitors for Human and Rat Steroid 5. ALPHA.-Reductases: Synthesis and Biological Evaluation of Indoline and Aniline Derivatives. III.

[Igarashi; Inami; Hara; Koutoku; Oritani; Mase Chemical and Pharmaceutical Bulletin, 2000 , vol. 48, # 11 p. 1689 - 1697]

More Articles...