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Volumn 32, Issue 25, 1991, Pages 2857-2860

Highly enantioselective routes to darzens and acetate aldol products from achiral aldehydes and t-butyl bromoacetate

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; ESTER;

ARTICLE; CHEMICAL STRUCTURE; PRIORITY JOURNAL; REACTION ANALYSIS; SYNTHESIS;

EID: 0025906950 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/0040-4039(91)80631-F Document Type: Article

Times cited : (94)

References (15)

2
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- For earlier studies see
- (1989) J. Am. Chem. Soc. , vol.111 , pp. 5493-5495
- Corey¹ Imwinkelried² Pikul³ Xiang⁴

3
- 0000584420
- For review see, J.D. Morrison, Academic Press
- (1984) Asymmetric Synthesis , vol.3 , pp. 111-212
- Heathcock¹

4
- 0002049209
- (1987) Tetrahedron Lett. , vol.28 , pp. 39-42
- Evans¹ Sjogren² Weber³ Conn⁴

6
- 0006388843
- Stereospecific Preparation of Transglycidic Esters
- (1989) Synthetic Communications , vol.19 , pp. 221-232
- Polniaszek¹ Belmont²

7
- 0001957688
- Stereoselective synthesis of cis-.ALPHA.,.BETA.-epoxyketones via divalent tin enolate.
- (1982) Chemistry Letters , pp. 1601-1604
- Mukaiyama¹ Haga² Iwasawa³

10
- 0000830198
- 3); see
- (1984) J. Org. Chem. , vol.49 , pp. 3707-3711
- Rossiter¹ Sharpless²

11
- 0000241934
- See also
- (1984) Tetrahedron Lett. , vol.25 , pp. 5031-5034
- Braun¹ Devant²

12
- 84973329202
- Stereoselective Aldol Reactions withα-Unsubstituted Chiral Enolates
- (1987) Angewandte Chemie International Edition in English , vol.26 , pp. 24-37
- Braun¹

14
- 84918629485
- A small amount (< 10%) of the α-epimeric azide diastereomer was formed in this process via α-deprotonation-reprotonation, a more serious side reaction under other conditions.

15
- 84918645816
- This research was assisted financially by a grant from the National Institutes of Health.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.