SCOPUS 정보 검색 플랫폼

Volumn 36, Issue 25, 1995, Pages 4447-4450

4M lithium perchlorate-nitromethane: An efficient solvent in Diels-Alder reactions using nitroalkenes as dienophiles

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; AROMATIC NITRO COMPOUND;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS;

BETULACEAE;

EID: 0029035367 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/0040-4039(95)00678-6 Document Type: Article

Times cited : (43)

References (18)

4
- 0000048258
- B.M. Trost, I. Fleming, L.A. Paquette, Pergamon, Oxford
- (1991) Comprehensive Organic Synthesis , vol.5 , pp. 315
- Oppolzer¹

5
- 0001628241
- See for example
- (1995) J. Am. Chem. Soc. , vol.117 , pp. 2100
- Denmark¹ Stolle² Dixon³ Guagnano⁴

7
- 0000494830
- (1990) J. Am. Chem. Soc. , vol.112 , pp. 4595
- Grieco¹ Nunes² Gaul³

8
- 33748224631
- (1991) Angew. Chem. Int. Ed. Engl. , vol.30 , pp. 1306
- Waldmann¹

13
- 84913984719
- 3, δ ppm): 7.26-7.21(m, 2H, =CH); 4.84-4.76(tt, 1H, J=6.7Hz, J′=1.4Hz, CHO); 4.32-4.24(dd, 1H, J=8.5Hz, J′=8.4Hz, HCHO); [[Truncated]]

15
- 84913984718
- 3, δppm): 138.2, 138.1, 128.3, 128.2, 127.7, 127.6, 127.5, 125.2, 124.3, 121.5, 121.3, 85.1, 84.5, 74.6, 72.5, 71.2, 70.7, [[Truncated]]

16
- 84913984717
- Although the structural assignment of diastereomers 7 and 8 is not univocally stablished at this stage of our research, we tentatively propose that the cycloadducts 7 are the major diastereomers, on the basis of previous studies for related chiral dienophiles. See
- (1994) Synlett , pp. 801
- Kant¹ Oikawa² Hosokawa³ Yanagiya⁴ Matsuda⁵ Shirahama⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.