cytotoxic sesquiterpenoids from eupatorium chinense

1
Additions and Corrections 2004, Volume 67 Sheng-Ping Yang, Jun Huo, Ying Wang, Li- Guang Lou, and Jian-Min Yue*: Cytotoxic Sesquiter- penoids from Eupatorium chinense. Page 642, column 1, paragraph 7, line 5: “deacetye- upaserrin (17) 10 ” should be revised as “mollisorin B (17) 9 ”. NP0402120 10.1021/np0402120 Published on Web 11/26/2004 2004, Volume 67 Jun Huo, Sheng-Ping Yang, Jian Ding, and Jian- Min Yue*: Cytotoxic Sesquiterpene Lactones from Eupato- rium lindleyanum. Page 1471, Chart 1: The structure of known compound 18 should be revised as follows, and its chemical name should be accordingly revised as 8-(4-hydroxytigloyloxy)- 3,14-dihydroxy-6H,7RH-germacra-1(10)Z,4E,11(13)-trien- 6,12-olide (18) throughout the paper. Page 1474, column 1, paragraph 2, line 7: “(18) 7 ” should be revised as “(18) 14 ”. Page 1475, References and Notes: ref 7 “Hernandez, L. R. Phytochemistry 1994, 37, 1331-1335.” should be revised as “Herna ´ ndez, L. R.; Catala ´ n, C. A. N.; Cerda-Garcı ´a- Rojas, C. M.; Joseph-Nathan, P. Phytochemistry 1994, 37, 1331-1335.” Page 1475, References and Notes: ref 14 “Hernandez, L. R. Phytochemistry 1996, 42,1369-1373.” should be revised as “Herna ´ ndez, L. R.; de Riscala, E. C.; Catala ´n, C. A. N.; Dı ´az, J. G.; Herz, W. Phytochemistry 1996, 42, 681-684.” NP0402118 10.1021/np0402118 Published on Web 11/26/2004 156 J. Nat. Prod. 2005, 68, 156

Upload: jian-min

Post on 10-Feb-2017

213 views

Category:

Documents


1 download

TRANSCRIPT

Page 1: Cytotoxic Sesquiterpenoids from               Eupatorium chinense

Additions and Corrections

2004, Volume 67

Sheng-Ping Yang, Jun Huo, Ying Wang, Li-Guang Lou, and Jian-Min Yue*: Cytotoxic Sesquiter-penoids from Eupatorium chinense.

Page 642, column 1, paragraph 7, line 5: “deacetye-upaserrin (17)10” should be revised as “mollisorin B (17)9”.

NP0402120

10.1021/np0402120Published on Web 11/26/2004

2004, Volume 67

Jun Huo, Sheng-Ping Yang, Jian Ding, and Jian-Min Yue*: Cytotoxic Sesquiterpene Lactones from Eupato-rium lindleyanum.

Page 1471, Chart 1: The structure of known compound18 should be revised as follows, and its chemical nameshould be accordingly revised as 8â-(4′-hydroxytigloyloxy)-3â,14-dihydroxy-6âH,7RH-germacra-1(10)Z,4E,11(13)-trien-6,12-olide (18) throughout the paper.

Page 1474, column 1, paragraph 2, line 7: “(18)7” shouldbe revised as “(18)14”.

Page 1475, References and Notes: ref 7 “Hernandez, L.R. Phytochemistry 1994, 37, 1331-1335.” should be revisedas “Hernandez, L. R.; Catalan, C. A. N.; Cerda-Garcıa-Rojas, C. M.; Joseph-Nathan, P. Phytochemistry 1994, 37,1331-1335.”

Page 1475, References and Notes: ref 14 “Hernandez,L. R. Phytochemistry 1996, 42,1369-1373.” should berevised as “Hernandez, L. R.; de Riscala, E. C.; Catalan,C. A. N.; Dıaz, J. G.; Herz, W. Phytochemistry 1996, 42,681-684.”

NP0402118

10.1021/np0402118Published on Web 11/26/2004

156 J. Nat. Prod. 2005, 68, 156