메뉴 건너뛰기




Volumn 59, Issue 8, 2011, Pages 4057-4061

Easy access to aroma active unsaturated γ-lactones by addition of modified titanium homoenolate to aldehydes

Author keywords

lactone; homo Reformatsky reaction; titanium homoenolate

Indexed keywords

DOUBLE BONDS; GOOD YIELD; ONE STEP; REFERENCE COMPOUNDS; REFORMATSKY REACTION;

EID: 79955023811     PISSN: 00218561     EISSN: 15205118     Source Type: Journal    
DOI: 10.1021/jf104711x     Document Type: Article
Times cited : (10)

References (17)
  • 1
    • 79954990983 scopus 로고
    • Alkyl lactones
    • 3 rd ed.; Allured: Wheaton, IL,; pp - 265.
    • Bedoukian, P. Z. Alkyl lactones. In Perfumery and Flavoring Synthetics, 3 rd ed.; Allured: Wheaton, IL, 1986; pp 256 - 265.
    • (1986) Perfumery and Flavoring Synthetics , pp. 256
    • Bedoukian, P.Z.1
  • 3
    • 0000647632 scopus 로고
    • Identification and synthesis of new γ-lactones from tuberose absolute (Polienthes tuberosa)
    • Maurer, B.; Hauser, A. Identification and synthesis of new γ-lactones from tuberose absolute (Polienthes tuberosa) Helv. Chim. Acta 1982, 65, 462-476
    • (1982) Helv. Chim. Acta , vol.65 , pp. 462-476
    • Maurer, B.1    Hauser, A.2
  • 4
    • 21144431608 scopus 로고    scopus 로고
    • The chafer pheromone buibuilactone and ant pyrazines are also produced by marine bacteria
    • DOI 10.1007/s10886-005-3553-9
    • Dickschat, J. S.; Wagner-Döbler, I.; Schulz, S. The chafer pheromone buibuilactone and ant pyrazines are also produced by bacteria J. Chem. Ecol. 2005, 31, 925-947 (Pubitemid 40876456)
    • (2005) Journal of Chemical Ecology , vol.31 , Issue.4 , pp. 925-947
    • Dickschat, J.S.1    Wagner-Dobler, I.2    Schulz, S.3
  • 6
  • 7
    • 37049104350 scopus 로고
    • Hydroformylation of 1,6-dienes with carbonylhydridotris(triphenylphosphosphine) rhodium
    • Grigg, R.; Reimer, G. J.; Wade, A. R. Hydroformylation of 1,6-dienes with carbonylhydridotris(triphenylphosphosphine) rhodium J. Chem. Soc., Perkin Trans. 1 1983, 1929-1935
    • (1983) J. Chem. Soc., Perkin Trans. 1 , pp. 1929-1935
    • Grigg, R.1    Reimer, G.J.2    Wade, A.R.3
  • 8
    • 0016583907 scopus 로고
    • Synthesis of 3 Z -nonenal and 3 Z,6 Z -nonadienal
    • Kajiwara, T.; Odake, Y.; Hatanaka, A. Synthesis of 3 Z -nonenal and 3 Z,6 Z -nonadienal Agric. Biol. Chem. 1975, 39, 1617-1621
    • (1975) Agric. Biol. Chem. , vol.39 , pp. 1617-1621
    • Kajiwara, T.1    Odake, Y.2    Hatanaka, A.3
  • 9
    • 0021558291 scopus 로고
    • The homoaldol reaction, or how to overcome problems of regio- and stereo-selectivity
    • Hoppe, D. The homoaldol reaction, or how to overcome problems of regio- and stereo-selectivity Angew. Chem., Int. Ed. Engl. 1984, 23, 932-948
    • (1984) Angew. Chem., Int. Ed. Engl. , vol.23 , pp. 932-948
    • Hoppe, D.1
  • 10
    • 33845282139 scopus 로고
    • Carbon-carbon bond-forming reactions of zinc homoenolate of esters. A novel three-carbon nucleophile with general synthetic utility
    • Nakamura, E.; Aoki, S.; Sekiya, K.; Oshino, H.; Kuwajima, I. Carbon-carbon bond-forming reactions of zinc homoenolate of esters. A novel three-carbon nucleophile with general synthetic utility J. Am. Chem. Soc. 1987, 109, 8056-8066
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 8056-8066
    • Nakamura, E.1    Aoki, S.2    Sekiya, K.3    Oshino, H.4    Kuwajima, I.5
  • 11
    • 1542628602 scopus 로고
    • Catalytic homo-Reformatsky reaction. Ambident chemical reactivities of the zinc homoenolate of propionate
    • Oshino, H.; Nakamura, E.; Kuwajima, I. Catalytic homo-Reformatsky reaction. Ambident chemical reactivities of the zinc homoenolate of propionate J. Org. Chem. 1985, 50, 2802-2804
    • (1985) J. Org. Chem. , vol.50 , pp. 2802-2804
    • Oshino, H.1    Nakamura, E.2    Kuwajima, I.3
  • 12
    • 33845279644 scopus 로고
    • Titanium(IV)-mediated aldol-type condensation of zinc esters and zinc ketones with carbonyl electrophiles
    • Ochiai, H.; Nishihara, T.; Tamaru, Y.; Yohida, Z. Titanium(IV)-mediated aldol-type condensation of zinc esters and zinc ketones with carbonyl electrophiles J. Org. Chem. 1988, 53, 1343-1344
    • (1988) J. Org. Chem. , vol.53 , pp. 1343-1344
    • Ochiai, H.1    Nishihara, T.2    Tamaru, Y.3    Yohida, Z.4
  • 13
    • 15144352918 scopus 로고
    • Trichlorotitanium and alkoxytitanium homoenolates. Preparation, characterization, and utilization for organic synthesis
    • Nakamura, E.; Oshino, H.; Kuwajima, I. Trichlorotitanium and alkoxytitanium homoenolates. Preparation, characterization, and utilization for organic synthesis J. Am. Chem. Soc. 1986, 108, 3745-3755
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 3745-3755
    • Nakamura, E.1    Oshino, H.2    Kuwajima, I.3
  • 14
    • 0042801401 scopus 로고
    • Metal homoenolate chemistry. Isolation and reactions of titanium homoenolates of esters
    • Nakamura, E.; Kuwajima, I. Metal homoenolate chemistry. Isolation and reactions of titanium homoenolates of esters J. Am. Chem. Soc. 1983, 105, 651-652
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 651-652
    • Nakamura, E.1    Kuwajima, I.2
  • 17
    • 0001171599 scopus 로고
    • Syntheses of pure (9 Z,11 Z), (9 E,11 E), (9 E,11 Z), and (9 Z,11 E)-9,11-hexadecadienals - Possible candidate pheromones
    • Svirskaya, P. I.; Maiti, S. N.; Jones, A. J.; Khouw, B.; Leznoff, C. C. Syntheses of pure (9 Z,11 Z), (9 E,11 E), (9 E,11 Z), and (9 Z,11 E)-9,11-hexadecadienals - possible candidate pheromones J. Chem. Ecol. 1984, 10, 795-807
    • (1984) J. Chem. Ecol. , vol.10 , pp. 795-807
    • Svirskaya, P.I.1    Maiti, S.N.2    Jones, A.J.3    Khouw, B.4    Leznoff, C.C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.