3H-苯并[E]茚合成路线

参考文献

Rendina, Victor L.; Goetz, Samantha A.; Neitzel, Angelika E.; Kaplan, Hilan Z.; Kingsbury, Jason S.
Tetrahedron Letters, 2012 , vol. 53, # 1 p. 15 - 18

150723-29-8

939-27-52-乙基萘+

232-55-33H-苯并[E]茚+

232-54-2+

136415-67-33-萘-2-基-丙醛

参考文献

Grissom, Janet Wisniewski; Klingberg, Detlef
Journal of Organic Chemistry, 1993 , vol. 58, # 24 p. 6559 - 6564

2320-32-3

86-73-7芴+

4944-94-92,3-二氢-1H-苯并[e]茚+

232-55-33H-苯并[E]茚+

232-54-2

参考文献

Petrov; Dokichev; Tolstikov
Russian Journal of Organic Chemistry, 1999 , vol. 35, # 10 p. 1553 - 1553

1694-19-51-甲氧基-4-((E)-苯乙烯基)-苯

6554-98-9反式-4-羟基芪+

232-55-33H-苯并[E]茚+

232-54-2

参考文献

Chu, Li-Tse; Yu, Pin-Chih; Wu, Bo-Jian; Liao, Ying-Chi; Chou, Chin-Hsing
Heterocycles, 2007 , vol. 71, # 1 p. 165 - 173

144152-89-6

232-55-33H-苯并[E]茚

参考文献

Brown, Roger F. C.; Eastwood, Frank W.; Smith, Cameron J.
Australian Journal of Chemistry, 1992 , vol. 45, # 8 p. 1315 - 1320

144152-91-0

232-55-33H-苯并[E]茚

参考文献

Brown, Roger F. C.; Eastwood, Frank W.; Smith, Cameron J.
Australian Journal of Chemistry, 1992 , vol. 45, # 8 p. 1315 - 1320

144152-90-9

232-55-33H-苯并[E]茚

参考文献

Brown, Roger F. C.; Eastwood, Frank W.; Smith, Cameron J.
Australian Journal of Chemistry, 1992 , vol. 45, # 8 p. 1315 - 1320

178-83-6

232-55-33H-苯并[E]茚

参考文献

Kotlyarevskii,I.L.; Zanina,A.S.
J. Gen. Chem. USSR (Engl. Transl.), 1961 , vol. 31, # 10 p. 3206 - 3214,2991 - 2997

80221-20-1

232-55-33H-苯并[E]茚

参考文献

Kotlyarevskii,I.L.; Zanina,A.S.
J. Gen. Chem. USSR (Engl. Transl.), 1961 , vol. 31, # 10 p. 3206 - 3214,2991 - 2997

21658-35-53-萘-2-丙酸

232-55-33H-苯并[E]茚

参考文献

Rendina, Victor L.; Goetz, Samantha A.; Neitzel, Angelika E.; Kaplan, Hilan Z.; Kingsbury, Jason S.
Tetrahedron Letters, 2012 , vol. 53, # 1 p. 15 - 18