STERIC COURSE OF THE REDUCTIONS OF 2-ALKYLTETRAHYDROPYRANONES

[1] MECHANISM OF N-HALOAMIDE PROMOTED ELECTROPHILIC ADDITIONS - HIGH REGION AND STEREOSELECTIVITY IN CONVERSION OF 2-TERT-BUTYL-3,6-DIHYDRO-2H-PYRAN INTO BROMOHYDRINS AND IN OPENING OF CORRESPONDING EPOXIDES [J]. TETRAHEDRON, 1977, 33 (17) : 2271 - 2275

[2] ANSELMI C, 1979, GAZZ CHIM ITAL, V109, P41

[3] CONCERNING STEREOCHEMISTRY OF REDUCTION OF CYCLOHEXANONES WITH COMPLEX METAL HYDRIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (16) : 5427 - 5428

[4] REGIOSELECTIVITY AND STEREOSELECTIVITY OF 3-MEMBERED RING-OPENING OF SOME 3,4-EPOXYTETRAHYDROPYRANS AND OF CORRESPONDING EPIBROMONIUM IONS [J]. TETRAHEDRON, 1974, 30 (22) : 4013 - 4020

[5] BERTI G, 1974, CHIM IND-MILAN, V56, P571

[6] Brown H. C., 1970, J AM CHEM SOC, V92, P709

[7] SELECTIVE REDUCTIONS .8. STEREOCHEMISTRY OF REDUCTION OF CYCLIC AND BICYCLIC KETONES BY ALKOXY-SUBSTITUTED LITHIUM ALUMINUM HYDRIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (24) : 5620 - &

[8] LITHIUM TRI-SEC-BUTYLBOROHYDRIDE - NEW REAGENT FOR REDUCTION OF CYCLIC AND BICYCLIC KETONES WITH SUPER STEREOSELECTIVITY - REMARKABLY SIMPLE AND PRACTICAL PROCEDURE FOR CONVERSION OF KETONES TO ALCOHOLS IN EXCEPTIONALLY HIGH STEREOCHEMICAL PURITY [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (20) : 7159 - +

[9] SELECTIVE REDUCTIONS .20. STEREOCHEMISTRY OF REDUCTION OF CYCLIC, BICYCLIC, AND POLYCYCLIC KETONES BY DIALKYLBORANES - SIMPLE, CONVENIENT PROCEDURE FOR REDUCTION OF KETONES TO CORRESPONDING ALCOHOLS WITH EXCEPTIONALLY HIGH STERIC CONTROL [J]. JOURNAL OF ORGANIC CHEMISTRY, 1974, 39 (12) : 1631 - 1636

[10] BROWN HC, 1979, TETRAHEDRON, V35, P561

[1] MECHANISM OF N-HALOAMIDE PROMOTED ELECTROPHILIC ADDITIONS - HIGH REGION AND STEREOSELECTIVITY IN CONVERSION OF 2-TERT-BUTYL-3,6-DIHYDRO-2H-PYRAN INTO BROMOHYDRINS AND IN OPENING OF CORRESPONDING EPOXIDES [J]. TETRAHEDRON, 1977, 33 (17) : 2271 - 2275

[2] ANSELMI C, 1979, GAZZ CHIM ITAL, V109, P41

[3] CONCERNING STEREOCHEMISTRY OF REDUCTION OF CYCLOHEXANONES WITH COMPLEX METAL HYDRIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1973, 95 (16) : 5427 - 5428

[4] REGIOSELECTIVITY AND STEREOSELECTIVITY OF 3-MEMBERED RING-OPENING OF SOME 3,4-EPOXYTETRAHYDROPYRANS AND OF CORRESPONDING EPIBROMONIUM IONS [J]. TETRAHEDRON, 1974, 30 (22) : 4013 - 4020

[5] BERTI G, 1974, CHIM IND-MILAN, V56, P571

[6] Brown H. C., 1970, J AM CHEM SOC, V92, P709

[7] SELECTIVE REDUCTIONS .8. STEREOCHEMISTRY OF REDUCTION OF CYCLIC AND BICYCLIC KETONES BY ALKOXY-SUBSTITUTED LITHIUM ALUMINUM HYDRIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (24) : 5620 - &

[8] LITHIUM TRI-SEC-BUTYLBOROHYDRIDE - NEW REAGENT FOR REDUCTION OF CYCLIC AND BICYCLIC KETONES WITH SUPER STEREOSELECTIVITY - REMARKABLY SIMPLE AND PRACTICAL PROCEDURE FOR CONVERSION OF KETONES TO ALCOHOLS IN EXCEPTIONALLY HIGH STEREOCHEMICAL PURITY [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (20) : 7159 - +

[9] SELECTIVE REDUCTIONS .20. STEREOCHEMISTRY OF REDUCTION OF CYCLIC, BICYCLIC, AND POLYCYCLIC KETONES BY DIALKYLBORANES - SIMPLE, CONVENIENT PROCEDURE FOR REDUCTION OF KETONES TO CORRESPONDING ALCOHOLS WITH EXCEPTIONALLY HIGH STERIC CONTROL [J]. JOURNAL OF ORGANIC CHEMISTRY, 1974, 39 (12) : 1631 - 1636

[10] BROWN HC, 1979, TETRAHEDRON, V35, P561