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Volumn 11, Issue 4, 2000, Pages 381-386

Cohalogenation of Limonene, Carvomenthene and Related Unsaturated Monoterpenic Alcohols

Author keywords

Cyclisation; Electrophilic addition reaction; Halohydrins; Terpenes and terpenoids

Indexed keywords


EID: 0034373164     PISSN: 01035053     EISSN: None     Source Type: Journal    
DOI: 10.1590/S0103-50532000000400010     Document Type: Article
Times cited : (21)

References (37)
  • 8
    • 37049120553 scopus 로고
    • Absolute configurations of substrates, (a) (R)-Limonene: Pawson, B. A.; Cheung, H. -C.; Gurbaxani, S.; Saucy, G. J. Chem. Soc. Chem. Commun. 1968, 1057. (b) (R)-Carvomenthene: Sakota, N.; Tanara, S. Bull. Chem. Soc. Jpn. 1911, 44, 485. (5R)-Carveols: Buckingham, J. (Ed.) Dictionary of Organic Compounds, 5th ed., Chapman and Hall; New York, 1982. p. 3415. (S)-α-Terpineol: Fuller, A. T.; Kenyon, J. J. Chem. Soc. 1924, 125, 2304. (e) (S)-Perillyl alcohol: Büchi, G.; Hofhneinz, W.; Paukstelis, J. V. J. Am. Chem. Soc. 1969, 91, 6473.
    • (1968) J. Chem. Soc. Chem. Commun. , pp. 1057
    • Pawson, B.A.1    Cheung, H.C.2    Gurbaxani, S.3    Saucy, G.4
  • 9
    • 37049120553 scopus 로고
    • Absolute configurations of substrates, (a) (R)-Limonene: Pawson, B. A.; Cheung, H. -C.; Gurbaxani, S.; Saucy, G. J. Chem. Soc. Chem. Commun. 1968, 1057. (b) (R)-Carvomenthene: Sakota, N.; Tanara, S. Bull. Chem. Soc. Jpn. 1911, 44, 485. (5R)-Carveols: Buckingham, J. (Ed.) Dictionary of Organic Compounds, 5th ed., Chapman and Hall; New York, 1982. p. 3415. (S)-α-Terpineol: Fuller, A. T.; Kenyon, J. J. Chem. Soc. 1924, 125, 2304. (e) (S)-Perillyl alcohol: Büchi, G.; Hofhneinz, W.; Paukstelis, J. V. J. Am. Chem. Soc. 1969, 91, 6473.
    • (1911) Bull. Chem. Soc. Jpn. , vol.44 , pp. 485
    • Sakota, N.1    Tanara, S.2
  • 10
    • 37049120553 scopus 로고
    • Chapman and Hall; New York
    • Absolute configurations of substrates, (a) (R)-Limonene: Pawson, B. A.; Cheung, H. -C.; Gurbaxani, S.; Saucy, G. J. Chem. Soc. Chem. Commun. 1968, 1057. (b) (R)-Carvomenthene: Sakota, N.; Tanara, S. Bull. Chem. Soc. Jpn. 1911, 44, 485. (5R)-Carveols: Buckingham, J. (Ed.) Dictionary of Organic Compounds, 5th ed., Chapman and Hall; New York, 1982. p. 3415. (S)-α-Terpineol: Fuller, A. T.; Kenyon, J. J. Chem. Soc. 1924, 125, 2304. (e) (S)-Perillyl alcohol: Büchi, G.; Hofhneinz, W.; Paukstelis, J. V. J. Am. Chem. Soc. 1969, 91, 6473.
    • (1982) Dictionary of Organic Compounds, 5th Ed. , pp. 3415
    • Buckingham, J.1
  • 11
    • 84918664847 scopus 로고
    • Absolute configurations of substrates, (a) (R)-Limonene: Pawson, B. A.; Cheung, H. -C.; Gurbaxani, S.; Saucy, G. J. Chem. Soc. Chem. Commun. 1968, 1057. (b) (R)-Carvomenthene: Sakota, N.; Tanara, S. Bull. Chem. Soc. Jpn. 1911, 44, 485. (5R)-Carveols: Buckingham, J. (Ed.) Dictionary of Organic Compounds, 5th ed., Chapman and Hall; New York, 1982. p. 3415. (S)-α-Terpineol: Fuller, A. T.; Kenyon, J. J. Chem. Soc. 1924, 125, 2304. (e) (S)-Perillyl alcohol: Büchi, G.; Hofhneinz, W.; Paukstelis, J. V. J. Am. Chem. Soc. 1969, 91, 6473.
    • (1924) J. Chem. Soc. , vol.125 , pp. 2304
    • Fuller, A.T.1    Kenyon, J.2
  • 12
    • 0001664608 scopus 로고
    • Absolute configurations of substrates, (a) (R)-Limonene: Pawson, B. A.; Cheung, H. -C.; Gurbaxani, S.; Saucy, G. J. Chem. Soc. Chem. Commun. 1968, 1057. (b) (R)-Carvomenthene: Sakota, N.; Tanara, S. Bull. Chem. Soc. Jpn. 1911, 44, 485. (5R)-Carveols: Buckingham, J. (Ed.) Dictionary of Organic Compounds, 5th ed., Chapman and Hall; New York, 1982. p. 3415. (S)-α-Terpineol: Fuller, A. T.; Kenyon, J. J. Chem. Soc. 1924, 125, 2304. (e) (S)-Perillyl alcohol: Büchi, G.; Hofhneinz, W.; Paukstelis, J. V. J. Am. Chem. Soc. 1969, 91, 6473.
    • (1969) J. Am. Chem. Soc. , vol.91 , pp. 6473
    • Büchi, G.1    Hofhneinz, W.2    Paukstelis, J.V.3
  • 13
    • 0000912147 scopus 로고
    • The trans isomer refers to the isomer with 1,4-dialkyl groups trans to each other (Royals, E. E.; Leffingwell, J. C. J. Org. Chem. 1966, 31, 1937).
    • (1966) J. Org. Chem. , vol.31 , pp. 1937
    • Royals, E.E.1    Leffingwell, J.C.2
  • 27
    • 85088903685 scopus 로고    scopus 로고
    • +•, 0.3), 278 (0.7), 151 (50), 123 (50), 109 (90), 43 (100)
    • +•, 0.3), 278 (0.7), 151 (50), 123 (50), 109 (90), 43 (100).
  • 34
    • 85088904849 scopus 로고    scopus 로고
    • +•, 1), 265 (5), 222 (2), 207 (1), 181 (1), 153 (41), 135 (19), 123 (1), 109 (10), 95 (100), 69 (14), 59 (57), 43 (59)
    • +•, 1), 265 (5), 222 (2), 207 (1), 181 (1), 153 (41), 135 (19), 123 (1), 109 (10), 95 (100), 69 (14), 59 (57), 43 (59).
  • 36
    • 85088887587 scopus 로고    scopus 로고
    • +•-H2O-I, 16), 281 (25), 263 (8), 235 (16), 209 (6), 169 (24), 167 (100), 149 (34), 121(27), 93 (89), 79 (50), 43 (30)
    • +•-H2O-I, 16), 281 (25), 263 (8), 235 (16), 209 (6), 169 (24), 167 (100), 149 (34), 121(27), 93 (89), 79 (50), 43 (30).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.