SCOPUS 정보 검색 플랫폼

Volumn 28, Issue 37, 1987, Pages 4303-4306

Synthesis of (±)-prepinnaterpene, a bromoditerpene from the red alga Laurencia Pinnata Yamada

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000519465 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)96491-8 Document Type: Article

Times cited : (69)

References (14)

2
- 0038762574
- Pinnaterpenes A,B,and C,new dibromoditerpenes from the red alga Laurencia pinnata Yamada.
- (1982) Chemistry Letters , pp. 1389
- Fukuzawa¹ Kumagai² Masamune³ Furusaki⁴ Matsumoto⁵ Katayama⁶

3
- 0011388253
- Structure of a new bromoditerpene, prepinnaterpene, from the marine red alga Laurencia pinnata Yamada.
- (1985) Chemistry Letters , pp. 1263
- Fukuzawa¹ Takaya² Matsue³ Masamune⁴

6
- 37049060307
- 672. Aspects of stereochemistry. Part X. The preparation and hydration of a ditertiary vicinal epoxide of the decalin series
- (1958) Journal of the Chemical Society (Resumed) , pp. 3293
- Henbest¹ Smith² Thomas³

8
- 84919145584
- The numbering of all synthetic perhydroindans refers to that of irieols.

9
- 84919145583
- 2, room temp, 1.5 h; v) NaOMe, MeOH, room temp, 21 h. NOE: 10-H → 5α-H, 6α-H, 8α-H for i: 10-H → 2α-H, 6α-H, 8α-H for ii.

11
- 84919145581
- The same bromination of the mesylate of 13 at 80 °C for 16 h gave a 1:4:3 mixture of 14, 15, and 13. This result suggested that 14 would be formed by double inversion of 13 via 15, and olefin 16 would be derived from 15.

13
- 0002241493
- Transformation of (-)-germacrene-D into (±)-oppositol (4), involving a biomimetic process, has recently been reported:
- (1986) Tetrahedron Lett. , vol.27 , pp. 57
- Shizuri¹ Yamaguchi² Terada³ Yamamura⁴

14
- 84919145580
- 3P, 100°C, 7 h; v) MeI, BuLi, room temp, 15 min; vi) LDA, THF, room temp, 2 h.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.