Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Raymond Shelden"'
Publikováno v:
Journal of the American Chemical Society. 92:1675-1681
Autor:
H. Raymond Shelden, Harold W. Moore
Publikováno v:
Tetrahedron Letters. 9:5431-5434
Autor:
H. Raymond Shelden, Harold W. Moore
Publikováno v:
The Journal of Organic Chemistry. 32:3603-3607
Publikováno v:
The Journal of Organic Chemistry. 33:998-1002
Publikováno v:
The Journal of Organic Chemistry. 43:2304-2306
Publikováno v:
The Journal of Organic Chemistry. 34:1999-2001
Publikováno v:
Moore, HW; Weyler, W; & Shelden, HR. (1969). Rearrangements of azidoquinones VI. Thermal rearrangement of azido-1,4-quinones to 2-cyano-1,3-cyclopentenediones. Tetrahedron Letters, 10(45), 3947-3950. doi: 10.1016/S0040-4039(01)88583-X. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/0xf4j329
Tetralledron Letters No.45, pPO 3947-3950, 1969. Pergamon Press. Printed in Great Britain. REARRANGEMENTS OF AZIDGQUINONlB VI. THERMAL REARRANGEMENT OF AZIDO-1, I-QUINONES TO 2-CYANO-1,3-CYCLOPENTENEDIONES Harold W. Moore, Walter Weyler, Jr., and II.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d501525abe98b648fdbc8e6d3c3ae993
http://www.escholarship.org/uc/item/0xf4j329
http://www.escholarship.org/uc/item/0xf4j329
Publikováno v:
Moore, HW; Shelden, HR; & Weyler, W. (1969). Rearrangement of azidoquinones IV. Ring expansion of 4-azido-1, 2-naphthoquinone. Tetrahedron Letters, 10(16), 1243-1246. doi: 10.1016/S0040-4039(01)87853-9. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/5h90k54m
Tetrahedron Letters No,L6, pg. 1243-1246, 1969. REARRANGEMENT Pergamon Pressu OF AZIDOQUINONES IV. RING EXPANSION OF 4-AZIDO-1, Harold W. Moore, Printed in Great Britain. P-NAPHTHOQUINONE H. Raymond Shelden and Walter Weyler Jr. Department of Chemist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2214a7910b5221134fbcfb1dab782410
http://www.escholarship.org/uc/item/5h90k54m
http://www.escholarship.org/uc/item/5h90k54m
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Die mit Schwefelsaure bzw. Trichloressigsaure katalysierte Umlagerung der Azidobenzo- (Ia) bzw. Azidonaphthochinone (Ib) fuhrt uber die Iminodiazoniumionen (IIa) bzw. (IIb) stereoselektiv bzw. stereospezifisch zu den Butenoliden (IIIa) bzw. (IIIb) mi
Autor:
H. Raymond Shelden
Publikováno v:
Journal of Chemical Education. 66:74
Semi-microscale experiments provide many advantages over macroscale work, including reduced cost of reagents, reduced waste generation, reduced vapors in lab, and increased safety.