SCOPUS 정보 검색 플랫폼

Volumn 33, Issue 51, 1992, Pages 7977-7980

Modification of π-face selectivity of 7-norbornenones during reduction in β-cyclodextrin and solid state

Author keywords

NaBH4 reduction solid state reaction.; cyclodextrin; Face selectivity

Indexed keywords

2 NORBORNEN 7 ONE DERIVATIVE; BETA CYCLODEXTRIN; NORBORNENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; PRIORITY JOURNAL; REDUCTION; SYNTHESIS;

EID: 0027053134 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)74793-9 Document Type: Article

Times cited : (25)

References (13)

1
- 0003979831
- For some general references see, Springer Verlag, New York
- (1978) Cyclodextrin Chemistry
- Bender¹ Komiyama²

3
- 0001024050
- (1992) Acc. Chem. Res. , vol.25 , pp. 299
- Ramamurthy¹ Eaton² Caspar³

8
- 30344431842
- Ground state geometric distortions distal substituent effects in determining the β-facial selectivity in 7-norbornenones
- (1992) Tetrahedron Letters , pp. 3069
- Kumar¹ Venkatesan² Ganguly³ Chandrasekhar⁴ Khan⁵ Mehta⁶

10
- 84914289404
- 2O) of the solid obtained on freeze drying a 1 : 1 mixture of the 7-norbornenone guest and β-CD host. However, the exact structure of this complex could not be established on the basis of the available evidence.

12
- 84990081452
- NaBH4 Reduction of Ketones in the Solid State
- 4 reductions see:
- (1989) Angewandte Chemie International Edition in English , vol.28 , pp. 320
- Toda¹ Kiyashige² Yagi³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.