Facile and efficient synthesis of homoallylic alcohols using allyl bromide and commercial zinc dust

Tetrahedron Letters

Volumn 36, Issue 27, 1995, Pages 4885-4888

  Ranu, Brindaban C ^a   Majee, Adinath ^a   Das, Asish R ^a  

^a DEPARTMENT OF MATERIALS SCIENCE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALKANOL; ALKENE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS;

EID: 85047674782     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/00404-0399(50)0877F-     Document Type: Article

References (24)

1. Addition of organochromium reagents to aldehydes, ketones and enones: a low-temperature version of the Nozaki?Hiyama reaction
2. Allylic sulfones as allyl anion equivalents: homoallylic alcohols from metal catalysed reactions of sulfones with aldehydes and ketones
3. Stereocontrolled synthesis of the hemibrevetoxin ring system via an allylic tin method
4. Diastereogenic Addition of Crotylmetal Compounds to Aldehydes
5. The Barbier Reaction - A One-Step Alternative for Syntheses via Organomagnesium Compounds
6. Tin-promoted stereocontrolled intramolecular allylation of carbonyl compounds: a facile and stereoselective method for ring construction
7. Magnesium- and titanium-induced reductive coupling of carbonyl compounds: efficient syntheses of pinacols and alkenes
8. Use of the Zn-Cu Couple in the Reformatsky Reaction
9. Allylzinc reagents additions in aqueous media
10. Zinc mediated allylation of aldehydes and ketones with cinnamyl chloride in aqueous medium