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1990, Vol. 62, Issue 10

Eighth International Conference on Organic Synthesis, Helsinki, Finland, 23–27 July 1990

This conference is part of the Organic Synthesis series.
Preface
T. A. Hase, J. Koskimies, G. Brunow and L. Koskinen
p. iv [Details] [Full text - pdf 60 kB]
Plenary Lectures
Enzyme mimics
R. Breslow
p. 1859 [Details] [Full text - pdf 610 kB]
Synthetic methodology involving the carbopalladation of allenes
Bernard Cazes
p. 1867 [Details] [Full text - pdf 579 kB]
Stereocontrol in organic synthesis using silicon compounds
I. Fleming
p. 1879 [Details] [Full text - pdf 575 kB]
The psychobiological basis of heuristic synthesis planning - man, machine and the chiron approach
S. Hanessian, Jonathan Franco and Benoit Larouche
p. 1887 [Details] [Full text - pdf 1816 kB]
Mechanistic investigations of a biomimetic polycyclization process that leads to the Daphniphyllum alkaloids
C. H. Heathcock, S. Piettre and John Kath
p. 1911 [Details] [Full text - pdf 437 kB]
CAMEO: a program for the logical prediction of the products of organic reactions
W. L. Jorgensen, E. R. Laird, A. J. Gushurst, J. M. Fleischer, S. A. Gothe, H. E. Helson, G. D. Paderes and S. Sinclair
p. 1921 [Details] [Full text - pdf 923 kB]
Synthetic applications of metallate rearrangements
P. Kocienski and Christopher Barber
p. 1933 [Details] [Full text - pdf 510 kB]
Regio- and stereocontrolled catalytic palladium- and nickel 'ene-type' cyclizations
W. Oppolzer
p. 1941 [Details] [Full text - pdf 341 kB]
New synthetic methodology using organosulfur compounds
G. H. Posner
p. 1949 [Details] [Full text - pdf 467 kB]
Invited Lectures
New perspectives of carbo- and hetero-l,3-dienes in organic synthesis
J. Barluenga, Fernando Aznar, S. Fustero and M. Tomas
p. 1957 [Details] [Full text - pdf 506 kB]
Synthesis of carbazole alkaloids
J. Bergman and B. Pelcman
p. 1967 [Details] [Full text - pdf 564 kB]
Synthetic routes proposed by a noninteractive synthesis program
T. Takabatake and Malcolm Bersohn
p. 1977 [Details] [Full text - pdf 137 kB]
Are flash pyrolytic reactions useful?
R. F. C. Brown
p. 1981 [Details] [Full text - pdf 288 kB]
Sequential cross-coupling reactions as a versatile synthetic tool
Vito Fiandanese
p. 1987 [Details] [Full text - pdf 349 kB]
Stereocontrol in allylboration reactions
R. W. Hoffmann, G. Niel and A. Schlapbach
p. 1993 [Details] [Full text - pdf 288 kB]
Metallated 2-alkenyl carbamates: chiral homoenolate reagents for asymmetric synthesis
D. Hoppe, Thomas Kramer, J.-R. Schwark and Oliver Zschage
p. 1999 [Details] [Full text - pdf 364 kB]
Methodology for stereochemical control in bioactive natural product synthesis - new methods toward enediyne antitumor antibiotics
M. Isobe, T. Nishikawa, Angkana Herunsalee, T. Tsukiyama, Yumi Hirose, K. Shimokawa and T. Goto
p. 2007 [Details] [Full text - pdf 267 kB]
Towards antibody-mediated metallo-porphyrin chemistry
E. Keinan, S. C. Sinha, A. Sinha-Bagchi, E. Benory, M. C. Ghozi, Z. Eshhar and B. S. Green
p. 2013 [Details] [Full text - pdf 481 kB]
α-silyl carbonyl compounds
G. L. Larson
p. 2021 [Details] [Full text - pdf 341 kB]
Catalysis of organic reactions by inorganic solids
P. Laszlo
p. 2027 [Details] [Full text - pdf 303 kB]
Stereoselective synthesis of inositol phosphates
S. V. Ley
p. 2031 [Details] [Full text - pdf 261 kB]
Intramolecular alkoxy-carbonylation of hydroxy alkenes promoted by Pd(II)
M. F. Semmelhack, Chung Kim, N. Zhang, C. Bodurow, M. Sanner, W. Dobler and M. Meier
p. 2035 [Details] [Full text - pdf 349 kB]
Chiral building blocks based on technical grade β-citronellene
E. P. Serebryakov, N. Cong Hao and M. V. Mavrov
p. 2041 [Details] [Full text - pdf 403 kB]
The directed ortho metalation reaction. Methodology, applications, synthetic links, and a non-aromatic ramification
V. Snieckus
p. 2047 [Details] [Full text - pdf 427 kB]
Transition metal-stabilised vinylketenes
L. Hill, C. J. Richards and S. E. Thomas
p. 2057 [Details] [Full text - pdf 350 kB]
Stereo- and regioselective organic transformations based on main group organometallic reagents - application to the stereocontrolled Claisen rearrangements
H. Yamamoto and K. Maruoka
p. 2063 [Details] [Full text - pdf 383 kB]