SCOPUS 정보 검색 플랫폼

Volumn 31, Issue 45, 1990, Pages 6509-6512

Stereoselective synthesis of (Z,E)-2-bromo-1,3-dienes via the palladium (O) catalyzed cross coupling reactions of 1,1-dibromoolefins and vinylboronic acids

(3) Roush, William R a Moriarty, Kevin J a Brown, Bradley B a

a INDIANA UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 BUTADIENE DERIVATIVE;

ARTICLE; NONHUMAN; PRIORITY JOURNAL; SYNTHESIS;

EID: 0025000356 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)97103-X Document Type: Article

Times cited : (116)

References (12)

1
- 0022343780
- (1985) Tetrahedron Lett. , vol.26 , pp. 4327
- Roush¹ Kageyama²

2
- 0000903259
- (1988) J. Org. Chem. , vol.53 , pp. 710
- Roush¹ Riva²

3
- 45549121429
- (1988) Tetrahedron Lett. , vol.29 , pp. 3541
- Roush¹ Brown² Drozda³

4
- 0022012266
- For leading references, see:
- (1985) J. Am. Chem. Soc. , vol.107 , pp. 972
- Miyaura¹ Yamada² Suginome³ Suzuki⁴

5
- 33845281635
- (1987) J. Am. Chem. Soc. , vol.109 , pp. 4756
- Uenishi¹ Beau² Armstrong³ Kishi⁴

6
- 33750283011
- (1989) J. Am. Chem. Soc. , vol.111 , pp. 314
- Miyaura¹ Ishiyama² Sasaki³ Ishikawa⁴ Satoh⁵ Suzuki⁶

7
- 0001425048
- (1986) Tetrahedron Lett. , vol.27 , pp. 2529
- Carpita¹ Rossi²

8
- 0001560769
- (1987) Tetrahedron Lett. , vol.28 , pp. 1649
- Ratovelomanana¹ Hammoud² Linstrumelle³

9
- 33845283423
- (1987) J. Am. Chem. Soc. , vol.109 , pp. 1257
- Minato¹ Suzuki² Tamao³

10
- 0001728170
- (an intramolecular cross coupling of a 1,1-dibromoolefin).
- (1987) J. Am. Chem. Soc. , vol.109 , pp. 3487
- Trost¹ Walchli²

11
- 0000344537
- Dibromoolefins 1, 4, 7, 8, 12, and 17 were synthesized from the corresponding aldehydes by use of the Corey-Fuchs dibromoolefination procedure:, The syntheses of 19 and especially 21 and 22 involve several operations after introduction of the dibromoolefin units, and will be described in detail elsewhere.
- (1972) Tetrahedron Lett. , pp. 3769
- Corey¹ Fuchs²

12
- 84918157923
- Vinylboronic acids 9 and 15 were prepared in 65–70% yields by hydroboration of the corresponding acetylenes with catecholborane (neat, 100°C) and were purified by silica gel chromatography.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.